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Cefuroxime
Cefuroxime - 0143-9979-22 - (Cefuroxime)
Drug Information of Cefuroxime
| Product NDC: | 0143-9979 |
| Proprietary Name: | Cefuroxime |
| Non Proprietary Name: | Cefuroxime |
| Active Ingredient(s): | 750 mg/1 & nbsp; Cefuroxime |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefuroxime
| Product NDC: | 0143-9979 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065048 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040109 |
Package Information of Cefuroxime
| Package NDC: | 0143-9979-22 |
| Package Description: | 25 INJECTION in 1 CARTON (0143-9979-22) |
NDC Information of Cefuroxime
| NDC Code | 0143-9979-22 |
| Proprietary Name | Cefuroxime |
| Package Description | 25 INJECTION in 1 CARTON (0143-9979-22) |
| Product NDC | 0143-9979 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefuroxime |
| Dosage Form Name | INJECTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20040109 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | CEFUROXIME SODIUM |
| Strength Number | 750 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
