Hydralazine Hydrochloride 68462-0341
Product NDC
68462-0341- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 29, 2009
- Listing Expires
- December 31, 2026
- Application
- ANDA090527
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydralazine Hydrochloride | 10 mg/1 |
Drug Class
Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(3)
100 TABLET in 1 BOTTLE (68462-341-01)
500 TABLET in 1 BOTTLE (68462-341-05)
1000 TABLET in 1 BOTTLE (68462-341-10)