Hydralazine Hydrochloride 23155-0835
Product NDC
23155-0835- Manufacturer
- Heritage Pharmaceuticals Inc. D/b/a Avet Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 2, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA040858
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydralazine Hydrochloride | 100 mg/1 |
Drug Class
Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (23155-835-01)