| NDC Code | 68645-604-54 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68645-604-54) |
|---|
| Product NDC | 68645-604 |
|---|
| 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 | 20051121 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077127 |
|---|
| Manufacturer | Legacy Pharmaceutical Packaging, LLC |
|---|
| Substance Name | NIFEDIPINE |
|---|
| Strength | 60 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
|---|