| NDC Code | 57664-664-83 |
|---|
| Package Description | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (57664-664-83) |
|---|
| Product NDC | 57664-664 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Carvedilol Phosphate |
|---|
| Non-Proprietary Name | Carvedilol Phosphate |
|---|
| Dosage Form | CAPSULE, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20171108 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090132 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | CARVEDILOL PHOSPHATE |
|---|
| Strength | 20 |
|---|
| 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] |
|---|