Product NDC: | 64679-713 |
Proprietary Name: | CEFPROZIL |
Non Proprietary Name: | CEFPROZIL |
Active Ingredient(s): | 500 mg/1 & nbsp; CEFPROZIL |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 64679-713 |
Labeler Name: | Wockhardt USA LLC. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065428 |
Marketing Category: | ANDA |
Start Marketing Date: | 20070615 |
Package NDC: | 64679-713-01 |
Package Description: | 50 TABLET, FILM COATED in 1 BOTTLE (64679-713-01) |
NDC Code | 64679-713-01 |
Proprietary Name | CEFPROZIL |
Package Description | 50 TABLET, FILM COATED in 1 BOTTLE (64679-713-01) |
Product NDC | 64679-713 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CEFPROZIL |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20070615 |
Marketing Category Name | ANDA |
Labeler Name | Wockhardt USA LLC. |
Substance Name | CEFPROZIL |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |