Hydralazine Hydrochloride 70518-4022
Product NDC
70518-4022- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 13, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA040858
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydralazine Hydrochloride | 10 mg/1 |
Drug Class
Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(2)
30 TABLET in 1 BLISTER PACK (70518-4022-0)
90 TABLET in 1 BOTTLE, PLASTIC (70518-4022-1)