| NDC Code | 53808-0329-1 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (53808-0329-1) |
|---|
| Product NDC | 53808-0329 |
|---|
| 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 | 20090701 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA073568 |
|---|
| Manufacturer | State of Florida DOH Central Pharmacy |
|---|
| Substance Name | VERAPAMIL HYDROCHLORIDE |
|---|
| Strength | 240 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | P-Glycoprotein Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA] |
|---|