| NDC Code: |
51079-467 |
| Proprietary Name: |
Felodipine |
| Suffix: |
|
| Non-Proprietary Name: |
Felodipine |
| Dosage Form: |
TABLET, FILM COATED, EXTENDED RELEASE |
| Method: |
ORAL |
| Original Marketing Date: |
22-10-2010 |
| Category Name: |
ANDA |
| Application Number: |
ANDA078855 |
| Labeler: |
UDL LABORATORIES, INC. |
| Substance Name: |
FELODIPINE |
| Active Numerator Strength: |
5 |
| Active Ingredient Unit: |
mg/1 |
| Pharm Classes: |
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |
| DEA Schedule: |
|
