Hydralazine Hydrochloride 70710-1988-07

Package NDC

70710-1988-07

Product NDC: 70710-1988

Manufacturer: Zydus Pharmaceuticals Usa Inc.
Dosage Form: Injection
Route: Intramuscular And Intravenous
Product Type: Human Prescription Drug
Marketing Start: April 28, 2025
Listing Expires: December 31, 2027
Application: ANDA202938

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Active Ingredients

Ingredient	Strength
Hydralazine Hydrochloride	20 mg/mL

Drug Class

Arteriolar Vasodilation [PE]Arteriolar Vasodilator [EPC]

Selected Package

70710-1988-07Selected

25 VIAL in 1 PACKAGE (70710-1988-7) / 1 mL in 1 VIAL (70710-1988-1)