NDC 64380-934 – LOSARTAN POTASSIUM 50 mg

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

Human Prescription Drug 4 recalls

Product NDC64380-934

Product details

Brand name
LOSARTAN POTASSIUM 50 mg
Generic name
Losartan Potassium
Labeler
Strides Pharma Science Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090382
Marketed since
October 9, 2019
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
64380-934-0430 TABLET, FILM COATED in 1 BOTTLE (64380-934-04)Oct 9, 2019
64380-934-0590 TABLET, FILM COATED in 1 BOTTLE (64380-934-05)Oct 9, 2019
64380-934-081000 TABLET, FILM COATED in 1 BOTTLE (64380-934-08)Oct 9, 2019

Recalls mentioning this NDC

Other Losartan potassium products