NDC 71205-598 – LOSARTAN POTASSIUM 50 mg

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

Human Prescription Drug

Product NDC71205-598

Product details

Brand name
LOSARTAN POTASSIUM 50 mg
Generic name
Losartan Potassium
Labeler
Proficient Rx LP
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090382
Marketed since
October 9, 2019
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
71205-598-3030 TABLET, FILM COATED in 1 BOTTLE (71205-598-30)Aug 10, 2021
71205-598-6060 TABLET, FILM COATED in 1 BOTTLE (71205-598-60)Aug 10, 2021
71205-598-9090 TABLET, FILM COATED in 1 BOTTLE (71205-598-90)Aug 10, 2021

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