| NDC Code | 68084-520-25 |
|---|
| Package Description | 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-520-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-520-95) |
|---|
| Product NDC | 68084-520 |
|---|
| 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 | 20110919 |
|---|
| End Marketing Date | 20180731 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA086242 |
|---|
| Manufacturer | American Health Packaging |
|---|
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC] |
|---|