Product NDC: | 16590-319 |
Proprietary Name: | NIFEDIPINE |
Non Proprietary Name: | NIFEDIPINE |
Active Ingredient(s): | 10 mg/1 & nbsp; NIFEDIPINE |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 16590-319 |
Labeler Name: | STAT RX USA LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA072579 |
Marketing Category: | ANDA |
Start Marketing Date: | 19890428 |
Package NDC: | 16590-319-20 |
Package Description: | 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (16590-319-20) |
NDC Code | 16590-319-20 |
Proprietary Name | NIFEDIPINE |
Package Description | 20 CAPSULE, LIQUID FILLED in 1 BOTTLE (16590-319-20) |
Product NDC | 16590-319 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | NIFEDIPINE |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 19890428 |
Marketing Category Name | ANDA |
Labeler Name | STAT RX USA LLC |
Substance Name | NIFEDIPINE |
Strength Number | 10 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |