Hydralazine Hydrochloride 51662-1648
Product NDC
51662-1648- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intramuscular And Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- June 30, 1997
- Listing Expires
- December 31, 2026
- Application
- ANDA040136
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Hydralazine Hydrochloride | 20 mg/mL |
Drug Class
Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]
Packaging Options(1)
25 POUCH in 1 CASE (51662-1648-3) / 1 VIAL, SINGLE-DOSE in 1 POUCH (51662-1648-2) / 1 mL in 1 VIAL, SINGLE-DOSE