| NDC Code | 68788-7330-9 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7330-9) |
|---|
| Product NDC | 68788-7330 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydralazine Hydrochloride |
|---|
| Non-Proprietary Name | Hydralazine Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190312 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA086242 |
|---|
| Manufacturer | Preferred Pharmaceuticals Inc. |
|---|
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
|---|