NDC 71610-563 – Montelukast

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

Human Prescription Drug

Product NDC71610-563

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
Aphena Pharma Solutions - Tennessee, LLC
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 (1)

Package NDCDescriptionSince
71610-563-3030 TABLET, FILM COATED in 1 BOTTLE (71610-563-30)May 27, 2021

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