Product NDC: | 67253-201 |
Proprietary Name: | Penicillin V Potassium |
Non Proprietary Name: | Penicillin V Potassium |
Active Ingredient(s): | 500 mg/1 & nbsp; Penicillin V Potassium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 67253-201 |
Labeler Name: | DAVA Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA062935 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040201 |
Package NDC: | 67253-201-50 |
Package Description: | 500 TABLET in 1 BOTTLE (67253-201-50) |
NDC Code | 67253-201-50 |
Proprietary Name | Penicillin V Potassium |
Package Description | 500 TABLET in 1 BOTTLE (67253-201-50) |
Product NDC | 67253-201 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Penicillin V Potassium |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20040201 |
Marketing Category Name | ANDA |
Labeler Name | DAVA Pharmaceuticals, Inc. |
Substance Name | PENICILLIN V POTASSIUM |
Strength Number | 500 |
Strength Unit | mg/1 |
Pharmaceutical Classes |