Ceftriaxone (Powder) Instructions for Use
ATC Code
J01DD04 (Ceftriaxone)
Active Substance
Ceftriaxone (Rec.INN registered by WHO)
Clinical-Pharmacological Group
Third generation cephalosporin
Pharmacotherapeutic Group
Systemic antibacterial agents; other beta-lactam antibacterial agents; third-generation cephalosporins
Pharmacological Action
A broad-spectrum cephalosporin antibiotic of the third generation. It exerts a bactericidal effect by inhibiting the synthesis of the bacterial cell wall.
Ceftriaxone acetylates membrane-bound transpeptidases, thereby disrupting the cross-linking of peptidoglycans, which is necessary to ensure the strength and rigidity of the cell wall.
It is active against aerobic, anaerobic, gram-positive and gram-negative bacteria.
It is resistant to the action of beta-lactamases.
Pharmacokinetics
Plasma protein binding is 85-95%.
Ceftriaxone is widely distributed in body tissues and fluids. Therapeutic concentrations are achieved in the cerebrospinal fluid in meningitis. High concentrations are achieved in bile. It crosses the placental barrier and is excreted in breast milk in small amounts.
About 40-65% of ceftriaxone is excreted unchanged in the urine. The remainder is excreted in bile and feces.
Indications
Infectious and inflammatory diseases caused by microorganisms sensitive to ceftriaxone, including peritonitis, sepsis, meningitis, cholangitis, gallbladder empyema, shigellosis, salmonella carriage, pneumonia, lung abscess, pleural empyema, pyelonephritis, infections of bones, joints, skin and soft tissues, genital organs, infected wounds and burns.
Prevention of postoperative infection.
ICD codes
| ICD-10 code | Indication |
| A01 | Typhoid and paratyphoid |
| A02 | Other salmonella infections |
| A03 | Shigellosis |
| A40 | Streptococcal sepsis |
| A41 | Other sepsis |
| G00 | Bacterial meningitis, not elsewhere classified |
| J15 | Bacterial pneumonia, not elsewhere classified |
| J85 | Abscess of lung and mediastinum |
| J86 | Pyothorax (pleural empyema) |
| K65.0 | Acute peritonitis (including abscess) |
| K81.0 | Acute cholecystitis |
| K81.1 | Chronic cholecystitis |
| K83.0 | Cholangitis |
| L01 | Impetigo |
| L02 | Cutaneous abscess, furuncle and carbuncle |
| L03 | Cellulitis |
| L08.0 | Pyoderma |
| L08.8 | Other specified local infections of skin and subcutaneous tissue |
| M00 | Pyogenic arthritis |
| M86 | Osteomyelitis |
| N10 | Acute tubulointerstitial nephritis (acute pyelonephritis) |
| N11 | Chronic tubulointerstitial nephritis (chronic pyelonephritis) |
| N30 | Cystitis |
| N34 | Urethritis and urethral syndrome |
| N41 | Inflammatory diseases of prostate |
| N70 | Salpingitis and oophoritis |
| N71 | Inflammatory disease of uterus, excluding cervix (including endometritis, myometritis, metritis, pyometra, uterine abscess) |
| N72 | Inflammatory disease of cervix uteri (including cervicitis, endocervicitis, exocervicitis) |
| N73.5 | Unspecified female pelvic peritonitis |
| T79.3 | Posttraumatic wound infection, not elsewhere classified |
| Z22.0 | Carrier of typhoid fever |
| Z29.2 | Other prophylactic chemotherapy (administration of antibiotics for prophylactic purposes) |
| ICD-11 code | Indication |
| 1A02 | Intestinal infections due to Shigella |
| 1A07.Z | Typhoid fever, unspecified |
| 1A08 | Paratyphoid fever |
| 1A09.Z | Salmonella infection, unspecified |
| 1B70.1 | Streptococcal cellulitis of the skin |
| 1B70.2 | Staphylococcal cellulitis of the skin |
| 1B70.Z | Bacterial cellulitis or lymphangitis caused by unspecified bacterium |
| 1B72.0 | Bullous impetigo |
| 1B72.1 | Nonbullous impetigo |
| 1B72.Z | Impetigo, unspecified |
| 1B75.0 | Furuncle |
| 1B75.1 | Carbuncle |
| 1B75.2 | Furunculosis |
| 1B75.3 | Pyogenic skin abscess |
| 1B7Y | Other specified pyogenic bacterial infections of skin or subcutaneous tissue |
| 1C44 | Non-pyogenic bacterial infections of skin |
| 1D01.0Z | Bacterial meningitis, unspecified |
| 1G40 | Sepsis without septic shock |
| CA40.0Z | Bacterial pneumonia, unspecified |
| CA43.Z | Abscess of lung or mediastinum, unspecified |
| CA44 | Pyothorax |
| DC12.0Z | Acute cholecystitis, unspecified |
| DC12.1 | Chronic cholecystitis |
| DC13 | Cholangitis |
| DC50.0 | Primary peritonitis |
| DC50.2 | Peritoneal abscess |
| DC50.Z | Peritonitis, unspecified |
| EA50.3 | Staphylococcal scarlet fever |
| EB21 | Pyoderma gangrenosum |
| FA1Z | Infectious arthropathies, unspecified |
| FB84.Z | Osteomyelitis or osteitis, unspecified |
| GA01.Z | Inflammatory diseases of uterus, except cervix, unspecified |
| GA05.2 | Unspecified pelvic peritonitis in women |
| GA07.Z | Salpingitis and oophoritis, unspecified |
| GA91.Z | Inflammatory and other diseases of prostate, unspecified |
| GB50 | Acute tubulo-interstitial nephritis |
| GB51 | Acute pyelonephritis |
| GB55.Z | Chronic tubulo-interstitial nephritis, unspecified |
| GB5Z | Renal tubulo-interstitial diseases, unspecified |
| GC00.Z | Cystitis, unspecified |
| GC02.Z | Urethritis and urethral syndrome, unspecified |
| NF0A.3 | Posttraumatic wound infection, not elsewhere classified |
| QC05.Y | Other specified prophylactic measures |
| QD00 | Carriage of Salmonella typhi |
| 1A0Z | Bacterial intestinal infections, unspecified |
| XN0QE | Salmonellae |
| GA0Z | Inflammatory diseases of female genital tract, unspecified |
| XA5WW1 | Cervix uteri |
Dosage Regimen
| The method of application and dosage regimen for a specific drug depend on its form of release and other factors. The optimal dosage regimen is determined by the doctor. It is necessary to strictly adhere to the compliance of the dosage form of a specific drug with the indications for use and dosage regimen. |
Powder
Individual. Administered intramuscularly or intravenously at 1-2 g every 24 hours or 0.5-1 g every 12 hours. Depending on the etiology of the disease, it can be administered intramuscularly at a dose of 250 mg once. The daily dose for newborns is 20-50 mg/kg; for children aged 2 months to 12 years – 20-100 mg/kg; frequency of administration is once a day. The duration of the course is determined individually. In patients with impaired renal function, adjustment of the dosing regimen is required, taking into account the creatinine clearance values.
Maximum daily doses for adults – 4 g, for children – 2 g.
Adverse Reactions
From the digestive system: nausea, vomiting, diarrhea, transient increase in the activity of liver transaminases, cholestatic jaundice, hepatitis, pseudomembranous colitis.
Allergic reactions: skin rash, itching, eosinophilia; rarely – angioedema.
From the hematopoietic system: with prolonged use in high doses, changes in the peripheral blood picture are possible (leukopenia, neutropenia, thrombocytopenia, hemolytic anemia).
From the blood coagulation system: hypoprothrombinemia.
From the urinary system: interstitial nephritis.
Effects due to chemotherapeutic action: candidiasis.
Local reactions: phlebitis (with intravenous administration), pain at the injection site (with intramuscular administration).
Contraindications
Hypersensitivity to ceftriaxone and other cephalosporins.
Use in Pregnancy and Lactation
Adequate and strictly controlled studies on the safety of ceftriaxone during pregnancy have not been conducted.
The use of ceftriaxone during pregnancy and lactation is possible in cases where the intended therapeutic benefit for the mother outweighs the potential risk to the fetus.
Ceftriaxone is excreted in breast milk in low concentrations.
In experimental animal studies, no teratogenic or embryotoxic effects of ceftriaxone were found.
Use in Renal Impairment
In patients with impaired renal function, adjustment of the dosing regimen is required, taking into account the creatinine clearance values.
Use with caution in severe renal impairment.
Pediatric Use
In newborns with hyperbilirubinemia, especially premature infants, use is possible under strict medical supervision.
Special Precautions
In patients with hypersensitivity to penicillins, allergic reactions to cephalosporin antibiotics are possible.
Use with caution in severe renal impairment.
Ceftriaxone solutions should not be mixed or administered simultaneously with other antimicrobial drugs or solutions.
In newborns with hyperbilirubinemia, especially premature infants, use is possible under strict medical supervision.
Drug Interactions
Ceftriaxone, by suppressing the intestinal flora, hinders the synthesis of vitamin K. Therefore, with simultaneous use with drugs that reduce platelet aggregation (NSAIDs, salicylates, sulfinpyrazone), the risk of bleeding increases. For the same reason, with simultaneous use with anticoagulants, an enhancement of the anticoagulant effect is noted.
With simultaneous use with “loop” diuretics, the risk of nephrotoxic effects increases.
Storage Conditions
Store at 2°C (36°F) to 25°C (77°F). Keep in original packaging, protected from light. Keep out of reach of children.
Dispensing Status
Rx Only
Important Safety Information
This information is for educational purposes only and does not replace professional medical advice. Always consult your doctor before use. Dosage and side effects may vary. Use only as prescribed.
Medical DisclaimerBrand (or Active Substance), Marketing Authorisation Holder, Dosage Form
Powder for solution for intravenous and intramuscular administration 1000 mg: fl. 1 or 10 pcs.
Marketing Authorization Holder
Fresenius Kabi Deutschland, GmbH (Germany)
Manufactured By
Labesfal-Laboratorios Almiro, S.A. (Portugal)
Dosage Form
| Ceftriaxone Kabi | Powder for solution for intravenous and intramuscular administration 1000 mg: fl. 1 or 10 pcs. |
Dosage Form, Packaging, and Composition
Powder for solution for intravenous and intramuscular administration almost white or yellowish in color, crystalline.
| 1 vial | |
| Ceftriaxone sodium sesquihydrate | 1193 mg, |
| Equivalent to ceftriaxone content | 1000 mg |
1000 mg – glass vials with a capacity of 15 ml (1) – cardboard packs.
1000 mg – glass vials with a capacity of 15 ml (10) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 500 mg: fl. 1 or 10 pcs.
Marketing Authorization Holder
Fresenius Kabi Deutschland, GmbH (Germany)
Manufactured By
Labesfal-Laboratorios Almiro, S.A. (Portugal)
Dosage Form
| Ceftriaxone Kabi | Powder for solution for intravenous and intramuscular administration 500 mg: fl. 1 or 10 pcs. |
Dosage Form, Packaging, and Composition
Powder for solution for intravenous and intramuscular administration almost white or yellowish in color, crystalline.
| 1 vial | |
| Ceftriaxone sodium sesquihydrate | 596.5 mg, |
| Equivalent to ceftriaxone content | 500 mg |
500 mg – glass vials with a capacity of 15 ml (1) – cardboard packs.
500 mg – glass vials with a capacity of 15 ml (10) – cardboard packs.
Powder for solution for infusions 2000 mg: vial 1 or 10 pcs.
Marketing Authorization Holder
Fresenius Kabi Deutschland, GmbH (Germany)
Manufactured By
Labesfal-Laboratorios Almiro, S.A. (Portugal)
Dosage Form
| Ceftriaxone Kabi | Powder for solution for infusions 2000 mg: vial 1 or 10 pcs. |
Dosage Form, Packaging, and Composition
Powder for solution for infusions almost white or yellowish, crystalline.
| 1 vial | |
| Ceftriaxone sodium sesquihydrate | 2386 mg, |
| Equivalent to ceftriaxone content | 2000 mg |
2000 mg – glass vials with a volume of 50 ml (1) – cardboard packs.
2000 mg – glass vials with a volume of 50 ml (10) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 2000 mg: vial 1 or 10 pcs.
Marketing Authorization Holder
Fresenius Kabi Deutschland, GmbH (Germany)
Manufactured By
Labesfal-Laboratorios Almiro, S.A. (Portugal)
Dosage Form
| Ceftriaxone Kabi | Powder for solution for intravenous and intramuscular administration 2000 mg: vial 1 or 10 pcs. |
Dosage Form, Packaging, and Composition
Powder for solution for intravenous and intramuscular administration almost white or yellowish in color, crystalline.
| 1 vial | |
| Ceftriaxone sodium sesquihydrate | 2386 mg, |
| Equivalent to ceftriaxone content | 2000 mg |
2000 mg – glass vials with a capacity of 15 ml (1) – cardboard packs.
2000 mg – glass vials with a capacity of 15 ml (10) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial 1 or 10 pcs.
Marketing Authorization Holder
Dominanta-Service, JSC (Russia)
Manufactured By
Fujian Fukang Pharmaceutical, Co. Ltd. (China)
Dosage Form
| Ceftriaxone Danhson | Powder for solution for intravenous and intramuscular administration 1 g: vial 1 or 10 pcs. |
Dosage Form, Packaging, and Composition
Powder for solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone (in the form of ceftriaxone sodium sesquihydrate) | 1 g |
1 g – glass vials with a capacity of 15 ml (1) – cardboard packs.
1 g – glass vials with a capacity of 15 ml (10) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc.
Marketing Authorization Holder
Dominanta-Service, JSC (Russia)
Manufactured By
Mekophar Chemical-Pharmaceutical, Joint Stock Company (Vietnam)
Dosage Form
| Ceftriaxone DS | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc. |
Dosage Form, Packaging, and Composition
| Powder for solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (in the form of sodium salt) | 1 g |
1 g – vials (1) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc.
Marketing Authorization Holder
Elfa SPC, JSC (Russia)
Manufactured By
Elfa Laboratories (India)
Dosage Form
| Ceftriaxone Elfa® | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
10 ml vials (1) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc.
Marketing Authorization Holder
Protech Biosystems, Pvt. Ltd. (India)
Dosage Form
| Ceftriaxone Protech | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
1 g – vials (1) – cardboard packs.
Powder for preparation of injection solution 250 mg: fl. 50 pcs.
Marketing Authorization Holder
Biokhimik, JSC (Russia)
Dosage Form
| Ceftriaxone sodium salt | Powder for preparation of injection solution 250 mg: fl. 50 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of injection solution from white to yellowish color.
| 1 vial | |
| Ceftriaxone (as sodium salt) | 250 mg |
250 mg – 10 ml vials (50) – cardboard boxes.
Powder for preparation of injection solution 500 mg: fl. 50 pcs.
Marketing Authorization Holder
Biokhimik, JSC (Russia)
Dosage Form
| Ceftriaxone sodium salt | Powder for preparation of injection solution 500 mg: fl. 50 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of injection solution from white to yellowish color.
| 1 vial | |
| Ceftriaxone (as sodium salt) | 500 mg |
500 mg – 10 ml vials (50) – cardboard boxes.
Powder for preparation of injection solution 1 g: fl. 50 pcs.
Marketing Authorization Holder
Biokhimik, JSC (Russia)
Dosage Form
| Ceftriaxone sodium salt | Powder for preparation of injection solution 1 g: fl. 50 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of injection solution from white to yellowish color.
| 1 vial | |
| Ceftriaxone (as sodium salt) | 1 g |
1 g – 10 ml vials (50) – cardboard boxes.
Powder for preparation of injection solution 2 g: fl. 50 pcs.
Marketing Authorization Holder
Biokhimik, JSC (Russia)
Dosage Form
| Ceftriaxone sodium salt | Powder for preparation of injection solution 2 g: fl. 50 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of injection solution from white to yellowish color.
| 1 vial | |
| Ceftriaxone (as sodium salt) | 2 g |
2 g – 10 ml vials (50) – cardboard boxes.
Powder for solution for intravenous and intramuscular administration 0.25 g: vial 1 or 10 pcs.
Marketing Authorization Holder
Binnopharm Group LLC (Russia)
Manufactured By
Sintez PJSC (Russia)
Dosage Form
| Ceftriaxone-AKOS | Powder for solution for intravenous and intramuscular administration 0.25 g: vial 1 or 10 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone (as ceftriaxone sodium) | 0.25 g |
0.25 g – glass vials (1) – cardboard packs.
0.25 g – glass vials (10) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 0.5 g: vial 1 or 10 pcs.
Powder for solution for intravenous and intramuscular administration 1 g: vial 1 or 10 pcs.
Powder for solution for intravenous and intramuscular administration 2 g: vial. 1 or 10 pcs.
Marketing Authorization Holder
Sintez PJSC (Russia)
Dosage Forms
| Ceftriaxone-Akos | Powder for solution for intravenous and intramuscular administration 0.5 g: vial 1 or 10 pcs. | |
| Powder for solution for intravenous and intramuscular administration 1 g: vial 1 or 10 pcs. | ||
| Powder for solution for intravenous and intramuscular administration 2 g: vial. 1 or 10 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone sodium | 0.535 g |
| Equivalent to ceftriaxone content | 0.5 g |
0.5 g – glass vials (1) with a capacity of 10 ml or 20 ml – cardboard packs.
0.5 g – glass vials (10) with a capacity of 10 ml or 20 ml – cardboard packs.
Powder for preparation of solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone sodium | 1.071 g |
| Equivalent to ceftriaxone content | 1 g |
1 g – glass vials (1) with a capacity of 10 ml or 20 ml – cardboard packs.
1 g – glass vials (10) with a capacity of 10 ml or 20 ml – cardboard packs.
Powder for preparation of solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone sodium | 2.142 g |
| Equivalent to ceftriaxone content | 2 g |
2 g – glass vials (1) with a capacity of 10 ml or 20 ml – cardboard packs.
2 g – glass vials (10) with a capacity of 10 ml or 20 ml – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc.
Marketing Authorization Holder
Alpa Expoim, LLC (Russia)
Manufactured By
Cooper Pharma (India)
Dosage Form
| Ceftriaxone-Alpa | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
1 g – vials (1) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc.
Marketing Authorization Holder
Darnitsa Pharmaceutical Firm, PJSC (Ukraine)
Dosage Form
| Ceftriaxone-Darnitsa | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
Vials (1) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 500 mg: fl. 1 pc.
Marketing Authorization Holder
Darnitsa Pharmaceutical Firm, PJSC (Ukraine)
Dosage Form
| Ceftriaxone-Darnitsa | Powder for solution for intravenous and intramuscular administration 500 mg: fl. 1 pc. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 500 mg |
Vials (1) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1, 10, 20, 25, 48, 50, or 100 pcs.
Marketing Authorization Holder
Jodas Expoim, LLC (Russia)
Manufactured By
Jodas Expoim, Pvt. Ltd. (India)
Or
Interpharma, LLC (Russia)
Dosage Form
| Ceftriaxone-Jodas | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1, 10, 20, 25, 48, 50, or 100 pcs. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
Vials (1) – cardboard boxes.
Vials (10) – cardboard boxes.
Vials (20) – cardboard boxes.
Vials (25) – cardboard boxes.
Vials (48) – cardboard boxes.
Vials (50) – cardboard boxes.
Vials (100) – cardboard boxes.
Powder for solution for intravenous and intramuscular administration 500 mg: vial 1, 10 or 40 pcs.
Marketing Authorization Holder
Alvils, LLC (Russia)
Dosage Form
| Ceftriaxone-KMP | Powder for solution for intravenous and intramuscular administration 500 mg: vial 1, 10 or 40 pcs. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 500 mg |
500 mg – vials (1) – cardboard packs.
500 mg – vials (10) – contour cell packs (1) – cardboard packs.
500 mg – vials (40) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial 1, 10 or 40 pcs.
Marketing Authorization Holder
Alvils, LLC (Russia)
Dosage Form
| Ceftriaxone-KMP | Powder for solution for intravenous and intramuscular administration 1 g: vial 1, 10 or 40 pcs. |
Dosage Form, Packaging, and Composition
| Powder for preparation of solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
1 g – vials (1) – cardboard packs.
1 g – vials (10) – contour cell packs (1) – cardboard packs.
1 g – vials (40) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc.
Marketing Authorization Holder
Protek-SVM LLC (Russia)
Manufactured By
Interpharma, LLC (Russia)
Or
Ruzpharma, LLC (Russia)
Dosage Form
| Ceftriaxone-LEKSVM® | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc. |
Dosage Form, Packaging, and Composition
Powder for preparation of solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone sodium sesquihydrate | 1193 mg, |
| Calculated as Ceftriaxone | 1000 mg |
1 g – glass vials (1) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 0.5 g: vial 1, 10, or 50 pcs.
Marketing Authorization Holder
Protek-SVM LLC (Russia)
Manufactured By
Redkinsky Pilot Plant, PJSC (Russia)
Dosage Form
| Ceftriaxone-LEKSVM | Powder for solution for intravenous and intramuscular administration 0.5 g: vial 1, 10, or 50 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone (as sodium salt) | 500 mg |
0.5 g – glass vials (1) – cardboard packs.
0.5 g – glass vials (10) – cardboard boxes.
0.5 g – glass vials (50) – cardboard boxes (for hospitals).
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1, 10, or 50 pcs.
Marketing Authorization Holder
Protek-SVM LLC (Russia)
Manufactured By
Redkinsky Pilot Plant, PJSC (Russia)
Labeled By
PROTEK-SVM, LLC (Russia)
Dosage Form
| Ceftriaxone-LEKSVM | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1, 10, or 50 pcs. |
Dosage Form, Packaging, and Composition
Powder for preparation of solution for intravenous and intramuscular administration white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone (as sodium salt) | 1000 mg |
1 g – glass vials (1) – cardboard packs.
1 g – glass vials (10) – cardboard boxes.
1 g – glass vials (50) – cardboard boxes (for hospitals).
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 or 50 pcs.
Marketing Authorization Holder
Promed Exports, Pvt. Ltd. (India)
Dosage Form
| Ceftriaxone-Promed | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 or 50 pcs. |
Dosage Form, Packaging, and Composition
Powder for solution for intravenous and intramuscular administration crystalline, white or white with a yellowish tint.
| 1 vial | |
| Ceftriaxone (as sodium salt) | 1 g |
1 g – Colorless glass vials with a capacity of 10 ml (1) – cardboard packs.
1 g – Colorless glass vials with a capacity of 10 ml (50) – cardboard boxes.
Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc.
Marketing Authorization Holder
Vial, LLC (Russia)
Manufactured By
NORTH CHINA PHARMACEUTICAL CORPORATION (China)
Dosage Form
| Ceftriaxone-Vial | Powder for solution for intravenous and intramuscular administration 1 g: vial. 1 pc. |
Dosage Form, Packaging, and Composition
| Powder for solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
1 g – vials (1) – cardboard packs.
Powder for solution for intravenous and intramuscular administration 1 g: fl. 1 pc. (packaged by Ozon LLC)
Marketing Authorization Holder
Vial, LLC (Russia)
Manufactured By
NORTH CHINA PHARMACEUTICAL CORPORATION (China)
Dosage Form
| Ceftriaxone-Vial | Powder for solution for intravenous and intramuscular administration 1 g: fl. 1 pc. (packaged by Ozon LLC) |
Dosage Form, Packaging, and Composition
| Powder for solution for intravenous and intramuscular administration | 1 vial |
| Ceftriaxone (as sodium salt) | 1 g |
Vials (1) – cardboard packs.
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