NDC 51655-918 – Losartan Potassium

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

Human Prescription Drug

Product NDC51655-918

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Northwind Health Company, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090083
Marketed since
March 2, 2022
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
51655-918-2690 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-918-26)Mar 2, 2022
51655-918-5230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-918-52)Mar 2, 2022

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