| NDC Code | 0517-0901-25 |
|---|
| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0901-25) > 1 mL in 1 VIAL, SINGLE-DOSE |
|---|
| Product NDC | 0517-0901 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Hydralazine Hydrochloride |
|---|
| Non-Proprietary Name | Hydralazine Hydrochloride |
|---|
| Dosage Form | INJECTION, SOLUTION |
|---|
| Usage | INTRAMUSCULAR; INTRAVENOUS |
|---|
| Start Marketing Date | 19970630 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA040136 |
|---|
| Manufacturer | American Regent, Inc. |
|---|
| Substance Name | HYDRALAZINE HYDROCHLORIDE |
|---|
| Strength | 20 |
|---|
| Strength Unit | mg/mL |
|---|
| Pharmacy Classes | Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC] |
|---|