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CEFADROXIL
CEFADROXIL - 16590-043-20 - (CEFADROXIL)
Drug Information of CEFADROXIL
| Product NDC: | 16590-043 |
| 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: | 16590-043 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065352 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070125 |
Package Information of CEFADROXIL
| Package NDC: | 16590-043-20 |
| Package Description: | 20 CAPSULE in 1 BOTTLE (16590-043-20) |
NDC Information of CEFADROXIL
| NDC Code | 16590-043-20 |
| Proprietary Name | CEFADROXIL |
| Package Description | 20 CAPSULE in 1 BOTTLE (16590-043-20) |
| Product NDC | 16590-043 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CEFADROXIL |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20070125 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| Substance Name | CEFADROXIL |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
