| NDC Code | 33342-374-12 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (33342-374-12) / 10 TABLET in 1 BLISTER PACK |
|---|
| Product NDC | 33342-374 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydralazine Hydrochloride |
|---|
| Non-Proprietary Name | Hydralazine Hydrochloride |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20240826 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA211010 |
|---|
| Manufacturer | Macleods Pharmaceuticals Limited |
|---|
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
|---|
| Strength | 10 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
|---|