Hydralazine Hydrochloride 00517-0901

Product NDC

00517-0901

Manufacturer: American Regent, Inc.
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)

00517-0901-25

25 VIAL, SINGLE-DOSE in 1 TRAY (0517-0901-25) / 1 mL in 1 VIAL, SINGLE-DOSE

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