NDC 69097-831 – Quinapril and Hydrochlorothiazide 20/25

Quinapril Hydrochloride 20 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69097-831

Product details

Brand name
Quinapril and Hydrochlorothiazide 20/25
Generic name
Quinapril and Hydrochlorothiazide 20/25
Labeler
Cipla USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA201356
Marketed since
July 20, 2016
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic

Active ingredients

Package NDC codes (1)

Package NDCDescriptionSince
69097-831-0590 TABLET in 1 BOTTLE (69097-831-05)Jul 20, 2016