NDC 68462-576 – Benazepril Hydrochloride and Hydrochlorothiazide

Benazepril Hydrochloride 5 mg/1; Hydrochlorothiazide 6.25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68462-576

Product details

Brand name
Benazepril Hydrochloride and Hydrochlorothiazide
Generic name
Benazepril Hydrochloride and Hydrochlorothiazide
Labeler
Glenmark Pharmaceuticals Inc., USA
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076631
Marketed since
March 17, 2015
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for benazepril hydrochloride and hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
68462-576-01100 TABLET, FILM COATED in 1 BOTTLE (68462-576-01)Dec 1, 2023

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