| NDC Code | 50228-184-10 |
|---|
| Package Description | 1000 TABLET in 1 BOTTLE (50228-184-10) |
|---|
| Product NDC | 50228-184 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydralazine Hydrochloride |
|---|
| Non-Proprietary Name | Hydralazine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170526 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA205236 |
|---|
| Manufacturer | ScieGen Pharmaceuticals, Inc. |
|---|
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
|---|