NDC 71335-0514 – Montelukast Sodium

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

Human Prescription Drug

Product NDC71335-0514

Product details

Brand name
Montelukast Sodium
Generic name
Montelukast Sodium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202717
Marketed since
April 11, 2013
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
71335-0514-130 TABLET, FILM COATED in 1 BOTTLE (71335-0514-1)Mar 8, 2018
71335-0514-24 TABLET, FILM COATED in 1 BOTTLE (71335-0514-2)Dec 27, 2021
71335-0514-37 TABLET, FILM COATED in 1 BOTTLE (71335-0514-3)Dec 27, 2021
71335-0514-460 TABLET, FILM COATED in 1 BOTTLE (71335-0514-4)Aug 29, 2018
71335-0514-510 TABLET, FILM COATED in 1 BOTTLE (71335-0514-5)Dec 27, 2021
71335-0514-690 TABLET, FILM COATED in 1 BOTTLE (71335-0514-6)Feb 12, 2018
71335-0514-7120 TABLET, FILM COATED in 1 BOTTLE (71335-0514-7)Apr 12, 2019
71335-0514-815 TABLET, FILM COATED in 1 BOTTLE (71335-0514-8)Dec 27, 2021

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