NDC 50090-4489 – Losartan Potassium

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

Human Prescription Drug

Product NDC50090-4489

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
A-S Medication Solutions
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 (3)

Package NDCDescriptionSince
50090-4489-030 TABLET, FILM COATED in 1 BOTTLE (50090-4489-0)Aug 29, 2019
50090-4489-190 TABLET, FILM COATED in 1 BOTTLE (50090-4489-1)Aug 29, 2019
50090-4489-2100 TABLET, FILM COATED in 1 BOTTLE (50090-4489-2)Aug 9, 2023

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