NDC 50268-556 – Montelukast

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

Human Prescription Drug

Product NDC50268-556

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
AvPAK
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202843
Marketed since
February 8, 2022
Listing expires
December 31, 2027
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Montelukast →

Package NDC codes (1)

Package NDCDescriptionSince
50268-556-1550 BLISTER PACK in 1 BOX (50268-556-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-556-11)Feb 8, 2022

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