NDC 71205-281 – Losartan Potassium

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

Human Prescription Drug

Product NDC71205-281

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090083
Marketed since
October 6, 2010
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Losartan potassium →

Package NDC codes (3)

Package NDCDescriptionSince
71205-281-3030 TABLET, FILM COATED in 1 BOTTLE (71205-281-30)Jun 1, 2019
71205-281-6060 TABLET, FILM COATED in 1 BOTTLE (71205-281-60)Jun 1, 2019
71205-281-9090 TABLET, FILM COATED in 1 BOTTLE (71205-281-90)Jun 1, 2019

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