NDC 50090-6108 – Montelukast

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

Human Prescription Drug

Product NDC50090-6108

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
A-S Medication Solutions
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202843
Marketed since
September 10, 2014
Listing expires
December 31, 2026
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Montelukast →

Package NDC codes (2)

Package NDCDescriptionSince
50090-6108-030 TABLET, FILM COATED in 1 BOTTLE (50090-6108-0)Sep 28, 2022
50090-6108-190 TABLET, FILM COATED in 1 BOTTLE (50090-6108-1)Sep 28, 2022

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