NDC 33342-045 – Losartan potassium

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

Human Prescription Drug 5 recalls

Product NDC33342-045

Product details

Brand name
Losartan potassium
Generic name
Losartan potassium
Labeler
Macleods Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202230
Marketed since
June 1, 2012
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 (4)

Package NDCDescriptionSince
33342-045-0730 TABLET, FILM COATED in 1 BOTTLE (33342-045-07)Jun 1, 2012
33342-045-1090 TABLET, FILM COATED in 1 BOTTLE (33342-045-10)Jun 1, 2012
33342-045-1210 BLISTER PACK in 1 CARTON (33342-045-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKJun 1, 2012
33342-045-441000 TABLET, FILM COATED in 1 BOTTLE (33342-045-44)Jan 18, 2016

Recalls mentioning this NDC

Other Losartan potassium products