NDC 43063-854 – Losartan Potassium

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

Human Prescription Drug 1 recall

Product NDC43063-854

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203835
Marketed since
August 19, 2015
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 (2)

Package NDCDescriptionSince
43063-854-6060 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-854-60)Jan 14, 2019
43063-854-9090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-854-90)May 29, 2018

Recalls mentioning this NDC

Other Losartan potassium products