NDC 72865-175 – Montelukast

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

Human Prescription Drug

Product NDC72865-175

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
XLCare Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202843
Marketed since
February 11, 2021
Listing expires
December 31, 2026
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Montelukast →

Package NDC codes (3)

Package NDCDescriptionSince
72865-175-101000 TABLET, FILM COATED in 1 BOTTLE (72865-175-10)Feb 11, 2021
72865-175-3030 TABLET, FILM COATED in 1 BOTTLE (72865-175-30)Feb 11, 2021
72865-175-9090 TABLET, FILM COATED in 1 BOTTLE (72865-175-90)Feb 11, 2021

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