Product NDC: | 60760-183 |
Proprietary Name: | NIFEDIPINE |
Non Proprietary Name: | NIFEDIPINE |
Active Ingredient(s): | 60 mg/1 & nbsp; NIFEDIPINE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60760-183 |
Labeler Name: | St Marys Medical Park Pharmacy |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077127 |
Marketing Category: | ANDA |
Start Marketing Date: | 20130515 |
Package NDC: | 60760-183-30 |
Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-183-30) |
NDC Code | 60760-183-30 |
Proprietary Name | NIFEDIPINE |
Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-183-30) |
Product NDC | 60760-183 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | NIFEDIPINE |
Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
Route Name | ORAL |
Start Marketing Date | 20130515 |
Marketing Category Name | ANDA |
Labeler Name | St Marys Medical Park Pharmacy |
Substance Name | NIFEDIPINE |
Strength Number | 60 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |