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ZINACEF
ZINACEF - 0173-0352-10 - (cefuroxime)
Drug Information of ZINACEF
| Product NDC: | 0173-0352 |
| Proprietary Name: | ZINACEF |
| Non Proprietary Name: | cefuroxime |
| Active Ingredient(s): | 750 mg/8.3mL & nbsp; cefuroxime |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ZINACEF
| Product NDC: | 0173-0352 |
| Labeler Name: | GlaxoSmithKline LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050558 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20041124 |
Package Information of ZINACEF
| Package NDC: | 0173-0352-10 |
| Package Description: | 10 VIAL in 1 TRAY (0173-0352-10) > 8.3 mL in 1 VIAL |
NDC Information of ZINACEF
| NDC Code | 0173-0352-10 |
| Proprietary Name | ZINACEF |
| Package Description | 10 VIAL in 1 TRAY (0173-0352-10) > 8.3 mL in 1 VIAL |
| Product NDC | 0173-0352 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cefuroxime |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20041124 |
| Marketing Category Name | NDA |
| Labeler Name | GlaxoSmithKline LLC |
| Substance Name | CEFUROXIME SODIUM |
| Strength Number | 750 |
| Strength Unit | mg/8.3mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
