| NDC Code | 0677-1980-01 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (0677-1980-01) > 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
|---|
| Product NDC | 0677-1980 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Nisoldipine |
|---|
| Non-Proprietary Name | Nisoldipine |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090901 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020356 |
|---|
| Manufacturer | United Research Laboratories, Inc. |
|---|
| Substance Name | NISOLDIPINE |
|---|
| Strength | 25.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Calcium Channel Antagonists [MoA],Decreased Blood Pressure [PE] |
|---|