| NDC Code: |
59762-6692 |
| Proprietary Name: |
nifedipine |
| Suffix: |
|
| Non-Proprietary Name: |
NIFEDIPINE |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
31-03-2010 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA019684 |
| Labeler: |
GREENSTONE LLC |
| Substance Name: |
NIFEDIPINE |
| Active Numerator Strength: |
90 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
| DEA Schedule: |
|
