NDC 68382-135 – Losartan Potassium

Losartan Potassium 25 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68382-135

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078243
Marketed since
October 4, 2010
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 (5)

Package NDCDescriptionSince
68382-135-01100 TABLET, FILM COATED in 1 BOTTLE (68382-135-01)Oct 4, 2010
68382-135-0630 TABLET, FILM COATED in 1 BOTTLE (68382-135-06)Oct 4, 2010
68382-135-101000 TABLET, FILM COATED in 1 BOTTLE (68382-135-10)Oct 4, 2010
68382-135-1690 TABLET, FILM COATED in 1 BOTTLE (68382-135-16)Oct 4, 2010
68382-135-2410000 TABLET, FILM COATED in 1 BOTTLE (68382-135-24)Oct 4, 2010

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