| NDC Code | 0172-4280-70 |
|---|
| Package Description | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0172-4280-70) |
|---|
| Product NDC | 0172-4280 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Verapamil Hydrochloride |
|---|
| Non-Proprietary Name | Verapamil Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 19920801 |
|---|
| End Marketing Date | 20150430 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA073568 |
|---|
| Manufacturer | IVAX Pharmaceuticals, Inc. |
|---|
| Substance Name | VERAPAMIL HYDROCHLORIDE |
|---|
| Strength | 240 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC] |
|---|