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Cefoxitin
Cefoxitin - 63323-342-25 - (Cefoxitin Sodium)
Drug Information of Cefoxitin
| Product NDC: | 63323-342 |
| Proprietary Name: | Cefoxitin |
| Non Proprietary Name: | Cefoxitin Sodium |
| Active Ingredient(s): | 2 g/1 & nbsp; Cefoxitin Sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | POWDER, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefoxitin
| Product NDC: | 63323-342 |
| Labeler Name: | APP Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065414 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110706 |
Package Information of Cefoxitin
| Package NDC: | 63323-342-25 |
| Package Description: | 25 VIAL in 1 CARTON (63323-342-25) > 1 POWDER, FOR SOLUTION in 1 VIAL |
NDC Information of Cefoxitin
| NDC Code | 63323-342-25 |
| Proprietary Name | Cefoxitin |
| Package Description | 25 VIAL in 1 CARTON (63323-342-25) > 1 POWDER, FOR SOLUTION in 1 VIAL |
| Product NDC | 63323-342 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefoxitin Sodium |
| Dosage Form Name | POWDER, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110706 |
| Marketing Category Name | ANDA |
| Labeler Name | APP Pharmaceuticals, LLC |
| Substance Name | CEFOXITIN SODIUM |
| Strength Number | 2 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
