| NDC Code | 72214-503-12 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72214-503-12) |
|---|
| Product NDC | 72214-503 |
|---|
| 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 | 20210101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA212016 |
|---|
| Manufacturer | Elite pharmaceutical Technology (Shanghai) Co., Ltd |
|---|
| Substance Name | NIFEDIPINE |
|---|
| Strength | 90 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
|---|