NDC 51655-418 – LOSARTAN POTASSIUM 50 mg

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

Human Prescription Drug

Product NDC51655-418

Product details

Brand name
LOSARTAN POTASSIUM 50 mg
Generic name
Losartan Potassium
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090382
Marketed since
July 15, 2020
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 (1)

Package NDCDescriptionSince
51655-418-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-418-26)Jul 15, 2020

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