NDC 31722-701 – Losartan Potassium

Losartan Potassium 50 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 3 recalls

Product NDC31722-701

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203835
Marketed since
August 19, 2015
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Losartan potassium →

Package NDC codes (5)

Package NDCDescriptionSince
31722-701-05500 TABLET, FILM COATED in 1 BOTTLE (31722-701-05)Aug 19, 2015
31722-701-101000 TABLET, FILM COATED in 1 BOTTLE (31722-701-10)Aug 19, 2015
31722-701-3030 TABLET, FILM COATED in 1 BOTTLE (31722-701-30)Aug 19, 2015
31722-701-6060 TABLET, FILM COATED in 1 BOTTLE (31722-701-60)Aug 19, 2015
31722-701-9090 TABLET, FILM COATED in 1 BOTTLE (31722-701-90)Aug 19, 2015

Recalls mentioning this NDC

Other Losartan potassium products