NDC 68180-376 – Losartan Potassium

Losartan Potassium 25 mg/1 · Tablet · Oral

Human Prescription Drug 3 recalls

Product NDC68180-376

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078232
Marketed since
November 1, 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 (2)

Package NDCDescriptionSince
68180-376-031000 TABLET in 1 BOTTLE (68180-376-03)Nov 1, 2017
68180-376-0990 TABLET in 1 BOTTLE (68180-376-09)Nov 1, 2017

Recalls mentioning this NDC

Other Losartan potassium products