Hydralazine Hydrochloride 70518-2551
Product NDC
70518-2551- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 22, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA040901
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydralazine Hydrochloride | 25 mg/1 |
Drug Class
Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(4)
30 TABLET in 1 BLISTER PACK (70518-2551-0)
30 TABLET in 1 BLISTER PACK (70518-2551-1)
180 TABLET in 1 BOTTLE, PLASTIC (70518-2551-2)
90 TABLET in 1 BOTTLE, PLASTIC (70518-2551-3)