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CEFOTAXIME
CEFOTAXIME - 64679-948-02 - (CEFOTAXIME)
Drug Information of CEFOTAXIME
| Product NDC: | 64679-948 |
| Proprietary Name: | CEFOTAXIME |
| Non Proprietary Name: | CEFOTAXIME |
| Active Ingredient(s): | 2 g/1 & nbsp; CEFOTAXIME |
| Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CEFOTAXIME
| Product NDC: | 64679-948 |
| Labeler Name: | WOCKHARDT USA LLC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065197 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080620 |
Package Information of CEFOTAXIME
| Package NDC: | 64679-948-02 |
| Package Description: | 10 CARTON in 1 CARTON (64679-948-02) > 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (64679-948-01) |
NDC Information of CEFOTAXIME
| NDC Code | 64679-948-02 |
| Proprietary Name | CEFOTAXIME |
| Package Description | 10 CARTON in 1 CARTON (64679-948-02) > 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (64679-948-01) |
| Product NDC | 64679-948 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFOTAXIME |
| Dosage Form Name | INJECTION, POWDER, FOR SOLUTION |
| Route Name | INTRAMUSCULAR; INTRAVENOUS |
| Start Marketing Date | 20080620 |
| Marketing Category Name | ANDA |
| Labeler Name | WOCKHARDT USA LLC. |
| Substance Name | CEFOTAXIME SODIUM |
| Strength Number | 2 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
