| NDC Code: |
50436-4068 |
| Proprietary Name: |
Nifedipine |
| Suffix: |
|
| Non-Proprietary Name: |
Nifedipine |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
21-11-2005 |
| Category Name: |
ANDA |
| Application Number: |
ANDA077127 |
| Labeler: |
UNIT DOSE SERVICES |
| Substance Name: |
NIFEDIPINE |
| Active Numerator Strength: |
30 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
| DEA Schedule: |
|
