NDC 65841-730 – Losartan Potassium

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

Human Prescription Drug

Product NDC65841-730

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078243
Marketed since
October 4, 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 (5)

Package NDCDescriptionSince
65841-730-01100 TABLET, FILM COATED in 1 BOTTLE (65841-730-01)Oct 4, 2010
65841-730-0630 TABLET, FILM COATED in 1 BOTTLE (65841-730-06)Oct 4, 2010
65841-730-101000 TABLET, FILM COATED in 1 BOTTLE (65841-730-10)Oct 4, 2010
65841-730-1690 TABLET, FILM COATED in 1 BOTTLE (65841-730-16)Oct 4, 2010
65841-730-2410000 TABLET, FILM COATED in 1 BOTTLE (65841-730-24)Oct 4, 2010

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