NDC 69097-829 – Quinapril and Hydrochlorothiazide 20/12.5

Quinapril Hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69097-829

Product details

Brand name
Quinapril and Hydrochlorothiazide 20/12.5
Generic name
Quinapril and Hydrochlorothiazide 20/12.5
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
69097-829-0590 TABLET in 1 BOTTLE (69097-829-05)Jul 20, 2016