NDC 23155-832 – Hydralazine Hydrochloride

Hydralazine Hydrochloride 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC23155-832

Product details

Brand name
Hydralazine Hydrochloride
Generic name
Hydralazine Hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040858
Marketed since
August 2, 2023
Listing expires
December 31, 2027
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

Uses, dosage, side effects and warnings for Hydralazine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
23155-832-01100 TABLET in 1 BOTTLE (23155-832-01)Aug 2, 2023
23155-832-101000 TABLET in 1 BOTTLE (23155-832-10)Aug 2, 2023

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