NDC 55154-2089 – Losartan Potassium

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

Human Prescription Drug

Product NDC55154-2089

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Cardinal Health 107, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078243
Marketed since
October 12, 2010
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
55154-2089-010 BLISTER PACK in 1 BAG (55154-2089-0) / 1 TABLET, FILM COATED in 1 BLISTER PACKOct 12, 2010

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