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Cefoxitin and Dextrose
Cefoxitin and Dextrose - 0264-3123-11 - (CEFOXITIN SODIUM)
Drug Information of Cefoxitin and Dextrose
| Product NDC: | 0264-3123 |
| Proprietary Name: | Cefoxitin and Dextrose |
| Non Proprietary Name: | CEFOXITIN SODIUM |
| Active Ingredient(s): | 1 g/50mL & nbsp; CEFOXITIN SODIUM |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefoxitin and Dextrose
| Product NDC: | 0264-3123 |
| Labeler Name: | B. Braun Medical Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA065214 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060310 |
Package Information of Cefoxitin and Dextrose
| Package NDC: | 0264-3123-11 |
| Package Description: | 24 CONTAINER in 1 CASE (0264-3123-11) > 50 mL in 1 CONTAINER |
NDC Information of Cefoxitin and Dextrose
| NDC Code | 0264-3123-11 |
| Proprietary Name | Cefoxitin and Dextrose |
| Package Description | 24 CONTAINER in 1 CASE (0264-3123-11) > 50 mL in 1 CONTAINER |
| Product NDC | 0264-3123 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFOXITIN SODIUM |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20060310 |
| Marketing Category Name | NDA |
| Labeler Name | B. Braun Medical Inc. |
| Substance Name | CEFOXITIN SODIUM |
| Strength Number | 1 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
