NDC 23155-003 – Hydralazine Hydrochloride

Hydralazine Hydrochloride 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC23155-003

Product details

Brand name
Hydralazine Hydrochloride
Generic name
Hydralazine hydrochloride
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA086242
Marketed since
April 6, 2007
Marketing end
September 30, 2026
Pharmacologic class
Arteriolar Vasodilator

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
23155-003-01100 TABLET, FILM COATED in 1 BOTTLE (23155-003-01)Apr 6, 2007
23155-003-101000 TABLET, FILM COATED in 1 BOTTLE (23155-003-10)Apr 6, 2007

Recalls mentioning this NDC

Other Hydralazine Hydrochloride products