| NDC Code | 23155-977-01 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (23155-977-01) / 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
|---|
| Product NDC | 23155-977 |
|---|
| 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 | 20260801 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA216606 |
|---|
| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
|---|
| Substance Name | NISOLDIPINE |
|---|
| Strength | 17 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
|---|