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Cefadroxil
Cefadroxil - 0093-4059-53 - (Cefadroxil)
Drug Information of Cefadroxil
| Product NDC: | 0093-4059 |
| Proprietary Name: | Cefadroxil |
| Non Proprietary Name: | Cefadroxil |
| Active Ingredient(s): | 1000 mg/1 & nbsp; Cefadroxil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefadroxil
| Product NDC: | 0093-4059 |
| Labeler Name: | Teva Pharmaceuticals USA Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062774 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070131 |
Package Information of Cefadroxil
| Package NDC: | 0093-4059-53 |
| Package Description: | 50 TABLET in 1 BOTTLE (0093-4059-53) |
NDC Information of Cefadroxil
| NDC Code | 0093-4059-53 |
| Proprietary Name | Cefadroxil |
| Package Description | 50 TABLET in 1 BOTTLE (0093-4059-53) |
| Product NDC | 0093-4059 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefadroxil |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070131 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Pharmaceuticals USA Inc |
| Substance Name | CEFADROXIL |
| Strength Number | 1000 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
