Hydralazine Hydrochloride 71335-2352
Product NDC
71335-2352- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 26, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA205236
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydralazine Hydrochloride | 25 mg/1 |
Drug Class
Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(5)
30 TABLET in 1 BOTTLE (71335-2352-1)
60 TABLET in 1 BOTTLE (71335-2352-2)
90 TABLET in 1 BOTTLE (71335-2352-3)
10 TABLET in 1 BOTTLE (71335-2352-4)
100 TABLET in 1 BOTTLE (71335-2352-5)