NDC 68788-8186 – Losartan Potassium

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

Human Prescription Drug

Product NDC68788-8186

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 6, 2022
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 (4)

Package NDCDescriptionSince
68788-8186-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8186-1)May 6, 2022
68788-8186-330 TABLET, FILM COATED in 1 BOTTLE (68788-8186-3)May 6, 2022
68788-8186-660 TABLET, FILM COATED in 1 BOTTLE (68788-8186-6)May 6, 2022
68788-8186-990 TABLET, FILM COATED in 1 BOTTLE (68788-8186-9)May 6, 2022

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