Home
>
National Drug Code (NDC)
>
Cefadroxil
Cefadroxil - 0143-9948-01 - (Cefadroxil)
Drug Information of Cefadroxil
| Product NDC: | 0143-9948 |
| Proprietary Name: | Cefadroxil |
| Non Proprietary Name: | Cefadroxil |
| Active Ingredient(s): | 1 g/1 & nbsp; Cefadroxil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefadroxil
| Product NDC: | 0143-9948 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065260 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20060330 |
Package Information of Cefadroxil
| Package NDC: | 0143-9948-01 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9948-01) |
NDC Information of Cefadroxil
| NDC Code | 0143-9948-01 |
| Proprietary Name | Cefadroxil |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0143-9948-01) |
| Product NDC | 0143-9948 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefadroxil |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20060330 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | CEFADROXIL |
| Strength Number | 1 |
| Strength Unit | g/1 |
| Pharmaceutical Classes | Cephalosporin Antibacterial [EPC],Cephalosporins [Chemical/Ingredient] |
