NDC 82009-042 – Losartan Potassium

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

Human Prescription Drug

Product NDC82009-042

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Quallent Pharmaceuticals Health LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078243
Marketed since
September 20, 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 (1)

Package NDCDescriptionSince
82009-042-101000 TABLET, FILM COATED in 1 BOTTLE (82009-042-10)Sep 20, 2022

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