NDC 46708-447 – Losartan Potassium

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

Human Prescription Drug

Product NDC46708-447

Product details

Brand name
Losartan Potassium
Generic name
Losartan Potassium
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090428
Marketed since
May 23, 2016
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
46708-447-3030 TABLET, FILM COATED in 1 BOTTLE (46708-447-30)May 23, 2016
46708-447-31100 TABLET, FILM COATED in 1 BOTTLE (46708-447-31)May 23, 2016
46708-447-9090 TABLET, FILM COATED in 1 BOTTLE (46708-447-90)May 23, 2016
46708-447-911000 TABLET, FILM COATED in 1 BOTTLE (46708-447-91)May 23, 2016

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