NDC 68788-8189 – Losartan Potassium

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

Human Prescription Drug

Product NDC68788-8189

Product details

Brand name
Losartan Potassium
Generic name
Losartan potassium
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA091497
Marketed since
May 13, 2022
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 (4)

Package NDCDescriptionSince
68788-8189-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8189-1)May 13, 2022
68788-8189-330 TABLET, FILM COATED in 1 BOTTLE (68788-8189-3)May 13, 2022
68788-8189-660 TABLET, FILM COATED in 1 BOTTLE (68788-8189-6)May 13, 2022
68788-8189-990 TABLET, FILM COATED in 1 BOTTLE (68788-8189-9)May 13, 2022

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