| NDC Code | 58118-0344-0 |
|---|
| Package Description | 1 TABLET in 1 PACKAGE (58118-0344-0) |
|---|
| Product NDC | 58118-0344 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydralazine Hydrochloride |
|---|
| Non-Proprietary Name | Hydralazine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090601 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090527 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
|---|