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Cefuroxime Sodium
Cefuroxime Sodium - 25021-119-20 - (Cefuroxime Sodium)
Drug Information of Cefuroxime Sodium
| Product NDC: | 25021-119 |
| Proprietary Name: | Cefuroxime Sodium |
| Non Proprietary Name: | Cefuroxime Sodium |
| Active Ingredient(s): | 1.5 g/16mL & nbsp; Cefuroxime Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefuroxime Sodium
| Product NDC: | 25021-119 |
| Labeler Name: | Sagent Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065048 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080501 |
Package Information of Cefuroxime Sodium
| Package NDC: | 25021-119-20 |
| Package Description: | 25 VIAL in 1 CARTON (25021-119-20) > 16 mL in 1 VIAL |
NDC Information of Cefuroxime Sodium
| NDC Code | 25021-119-20 |
| Proprietary Name | Cefuroxime Sodium |
| Package Description | 25 VIAL in 1 CARTON (25021-119-20) > 16 mL in 1 VIAL |
| Product NDC | 25021-119 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefuroxime Sodium |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20080501 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceuticals |
| Substance Name | CEFUROXIME SODIUM |
| Strength Number | 1.5 |
| Strength Unit | g/16mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
