| NDC Code | 0603-3583-21 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0603-3583-21) |
|---|
| Product NDC | 0603-3583 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Felodipine |
|---|
| Non-Proprietary Name | Felodipine |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20111215 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA200815 |
|---|
| Manufacturer | Par Pharmaceutical, Inc. |
|---|
| Substance Name | FELODIPINE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
|---|