| NDC Code | 68788-9885-9 |
|---|
| Package Description | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-9885-9) |
|---|
| Product NDC | 68788-9885 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Nifedipine |
|---|
| Non-Proprietary Name | Nifedipine |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20150423 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090649 |
|---|
| Manufacturer | Preferred Pharmaceuticals, Inc. |
|---|
| Substance Name | NIFEDIPINE |
|---|
| Strength | 60 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS] |
|---|