NDC 71610-838 – Lisinopril and Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71610-838

Product details

Brand name
Lisinopril and Hydrochlorothiazide
Generic name
Lisinopril and Hydrochlorothiazide
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077912
Marketed since
October 4, 2006
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Lisinopril and Hydrochlorothiazide →

Package NDC codes (5)

Package NDCDescriptionSince
71610-838-3030 TABLET in 1 BOTTLE (71610-838-30)May 31, 2024
71610-838-5360 TABLET in 1 BOTTLE (71610-838-53)May 31, 2024
71610-838-6090 TABLET in 1 BOTTLE (71610-838-60)May 31, 2024
71610-838-70120 TABLET in 1 BOTTLE (71610-838-70)May 31, 2024
71610-838-80180 TABLET in 1 BOTTLE (71610-838-80)May 31, 2024

Other Lisinopril and Hydrochlorothiazide products