Ceftriaxone Sodium Injection
Baxter Healthcare
Open FDA's page for this record- Discontinued date
- 10/30/2026
- Update type
- New
- Initial posting date
- 10/30/2026
- Package NDC
- 0338-5002-41
- Generic name
- Ceftriaxone Sodium Injection
- Contact info
- 888-229-0001
- Related info
- Discontinuation of the manufacture of the drug
- Update date
- 10/30/2026
- Dosage form
- Injection
- Presentation
- Ceftriaxone Sodium in Plastic Container, Injection, 1g/50mL (NDC 0338-5002-41)
- Company name
- Baxter Healthcare
- Status
- To Be Discontinued
- Therapeutic category
- Anti-Infective
- Harmonized identifiers (openFDA)
- Application number
- ANDA065224
- Brand name
- CEFTRIAXONE
- Generic name
- CEFTRIAXONE SODIUM
- Manufacturer name
- Baxter Healthcare Company
- Product NDC
- 0338-5002, 0338-5003
- Product type
- HUMAN PRESCRIPTION DRUG
- Route
- INTRAVENOUS
- Substance name
- CEFTRIAXONE SODIUM
- RxCUI
- 1665021, 1665046
- SPL ID
- e6debc12-1f25-437c-970e-607f4953c7f7
- SPL set ID
- 4c5c2d3f-5038-41a1-a2fe-4dcd048dbac1
- Package NDC
- 0338-5002-41, 0338-5003-41
- UNII
- 023Z5BR09K