NDC 33342-044 – Losartan potassium

Losartan Potassium 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 5 recalls

Product NDC33342-044

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
May 10, 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
33342-044-0730 TABLET, FILM COATED in 1 BOTTLE (33342-044-07)May 10, 2012
33342-044-1090 TABLET, FILM COATED in 1 BOTTLE (33342-044-10)May 10, 2012
33342-044-1210 BLISTER PACK in 1 CARTON (33342-044-12) / 10 TABLET, FILM COATED in 1 BLISTER PACKMay 10, 2012
33342-044-441000 TABLET, FILM COATED in 1 BOTTLE (33342-044-44)Jan 18, 2016

Recalls mentioning this NDC

Other Losartan potassium products