NDC 72888-220 – Benazepril hydrochloride and hydrochlorothiazide

Benazepril Hydrochloride 10 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72888-220

Product details

Brand name
Benazepril hydrochloride and hydrochlorothiazide
Generic name
Benazepril hydrochloride and hydrochlorothiazide
Labeler
Advagen Pharma Ltd
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA020033
Marketed since
December 5, 2024
Listing expires
December 31, 2027
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
72888-220-01100 TABLET in 1 BOTTLE (72888-220-01)Dec 5, 2024

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