NDC 0781-5560 – Montelukast

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

Human Prescription Drug

Product NDC0781-5560

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
Sandoz Inc
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200889
Marketed since
August 3, 2012
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
0781-5560-1310 BLISTER PACK in 1 CARTON (0781-5560-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5560-06)Jun 13, 2025
0781-5560-3130 TABLET, FILM COATED in 1 BOTTLE (0781-5560-31)Jun 13, 2025
0781-5560-9290 TABLET, FILM COATED in 1 BOTTLE (0781-5560-92)Jun 13, 2025

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