NDC 71335-1995 – Montelukast sodium

Montelukast Sodium 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-1995

Product details

Brand name
Montelukast sodium
Generic name
Montelukast sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204290
Marketed since
January 1, 2016
Listing expires
December 31, 2026
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Montelukast Sodium →

Package NDC codes (8)

Package NDCDescriptionSince
71335-1995-130 TABLET, FILM COATED in 1 BOTTLE (71335-1995-1)Dec 16, 2021
71335-1995-24 TABLET, FILM COATED in 1 BOTTLE (71335-1995-2)Apr 3, 2024
71335-1995-37 TABLET, FILM COATED in 1 BOTTLE (71335-1995-3)Apr 3, 2024
71335-1995-460 TABLET, FILM COATED in 1 BOTTLE (71335-1995-4)May 9, 2022
71335-1995-510 TABLET, FILM COATED in 1 BOTTLE (71335-1995-5)Apr 3, 2024
71335-1995-690 TABLET, FILM COATED in 1 BOTTLE (71335-1995-6)Dec 8, 2021
71335-1995-7120 TABLET, FILM COATED in 1 BOTTLE (71335-1995-7)Apr 3, 2024
71335-1995-815 TABLET, FILM COATED in 1 BOTTLE (71335-1995-8)Apr 3, 2024

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