NDC 70518-0718 – Losartan Potassium

Losartan Potassium 100 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC70518-0718

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
August 30, 2017
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 (3)

Package NDCDescriptionSince
70518-0718-030 TABLET, FILM COATED in 1 BLISTER PACK (70518-0718-0)Aug 30, 2017
70518-0718-190 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-1)Jul 20, 2018
70518-0718-3100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0718-3)Mar 20, 2025

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