Home
>
National Drug Code (NDC)
>
Cefadroxil
Cefadroxil - 0781-2938-01 - (Cefadroxil)
Drug Information of Cefadroxil
| Product NDC: | 0781-2938 |
| Proprietary Name: | Cefadroxil |
| Non Proprietary Name: | Cefadroxil |
| Active Ingredient(s): | 500 mg/1 & nbsp; Cefadroxil |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cefadroxil
| Product NDC: | 0781-2938 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA062291 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19800730 |
Package Information of Cefadroxil
| Package NDC: | 0781-2938-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (0781-2938-01) |
NDC Information of Cefadroxil
| NDC Code | 0781-2938-01 |
| Proprietary Name | Cefadroxil |
| Package Description | 100 CAPSULE in 1 BOTTLE (0781-2938-01) |
| Product NDC | 0781-2938 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Cefadroxil |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 19800730 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | CEFADROXIL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
