| NDC Code: |
66993-475 |
| Proprietary Name: |
Nisoldipine |
| Suffix: |
|
| Non-Proprietary Name: |
Nisoldipine |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
27-02-2012 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA020356 |
| Labeler: |
PRASCO LABORATORIES |
| Substance Name: |
NISOLDIPINE |
| Active Numerator Strength: |
34 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE] |
| DEA Schedule: |
|
