NDC 70518-3133 – Montelukast

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

Human Prescription Drug

Product NDC70518-3133

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202843
Marketed since
June 18, 2021
Listing expires
December 31, 2027
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Montelukast →

Package NDC codes (3)

Package NDCDescriptionSince
70518-3133-090 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3133-0)Jun 18, 2021
70518-3133-130 TABLET, FILM COATED in 1 BLISTER PACK (70518-3133-1)Jul 1, 2021
70518-3133-230 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3133-2)Aug 27, 2025

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