Composition
- Active ingredients
- CEFUROXIME SODIUM EQ 7.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- CEFUROXIME SODIUM EQ 1.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA050558-003 · Discontinued
- CEFUROXIME SODIUM EQ 7.5GM BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableThis page
- CEFUROXIME SODIUM EQ 750MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA050558-002 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application NDA050558.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Zinacef
- Active substance
- cefuroxime sodium
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Pai Holdings Pharm
- Status
- Discontinued
- FDA approval
- 19 Oct 1983
- Application
- NDA050558-004