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MEFOXIN
MEFOXIN - 67457-216-50 - (cefoxitin sodium)
Drug Information of MEFOXIN
| Product NDC: | 67457-216 |
| Proprietary Name: | MEFOXIN |
| Non Proprietary Name: | cefoxitin sodium |
| Active Ingredient(s): | 2 g/50mL & nbsp; cefoxitin sodium |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MEFOXIN
| Product NDC: | 67457-216 |
| Labeler Name: | Bioniche Pharma USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA063182 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110222 |
Package Information of MEFOXIN
| Package NDC: | 67457-216-50 |
| Package Description: | 24 BAG in 1 BOX (67457-216-50) > 50 mL in 1 BAG |
NDC Information of MEFOXIN
| NDC Code | 67457-216-50 |
| Proprietary Name | MEFOXIN |
| Package Description | 24 BAG in 1 BOX (67457-216-50) > 50 mL in 1 BAG |
| Product NDC | 67457-216 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | cefoxitin sodium |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20110222 |
| Marketing Category Name | ANDA |
| Labeler Name | Bioniche Pharma USA LLC |
| Substance Name | CEFOXITIN SODIUM |
| Strength Number | 2 |
| Strength Unit | g/50mL |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
