| NDC Code | 53808-0693-2 |
|---|
| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0693-2) |
|---|
| Product NDC | 53808-0693 |
|---|
| 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 | 20130101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077127 |
|---|
| Manufacturer | State of Florida DOH Central Pharmacy |
|---|
| Substance Name | NIFEDIPINE |
|---|
| Strength | 30 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS] |
|---|