| NDC Code | 70934-707-60 |
|---|
| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-707-60) |
|---|
| Product NDC | 70934-707 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Carvedilol |
|---|
| Non-Proprietary Name | Carvedilol |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200518 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA078251 |
|---|
| Manufacturer | Denton Pharma, Inc. dba Northwind Pharmaceuticals |
|---|
| Substance Name | CARVEDILOL |
|---|
| Strength | 12.5 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Adrenergic alpha-Antagonists [MoA], Adrenergic beta1-Antagonists [MoA], Adrenergic beta2-Antagonists [MoA], alpha-Adrenergic Blocker [EPC], beta-Adrenergic Blocker [EPC] |
|---|