NDC 70518-2316 – Losartan Potassium

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

Human Prescription Drug

Product NDC70518-2316

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090083
Marketed since
September 18, 2019
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 (2)

Package NDCDescriptionSince
70518-2316-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2316-1)Feb 14, 2024
70518-2316-2100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2316-2)Mar 20, 2025

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