Hydralazine Hydrochloride 50111-0327
Product NDC
50111-0327- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 30, 1990
- Listing Expires
- December 31, 2026
- Application
- ANDA088467
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydralazine Hydrochloride | 25 mg/1 |
Drug Class
Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(2)
100 TABLET in 1 BOTTLE (50111-327-01)
1000 TABLET in 1 BOTTLE (50111-327-03)