Hydralazine Hydrochloride 51662-1648-03

Package NDC

51662-1648-03

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]

Selected Package

51662-1648-03Selected

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