NDC 68071-5278 – Montelukast sodium

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

Human Prescription Drug

Product NDC68071-5278

Product details

Brand name
Montelukast sodium
Generic name
Montelukast sodium
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204290
Marketed since
January 1, 2016
Listing expires
December 31, 2026
Pharmacologic class
Leukotriene Receptor Antagonist

Active ingredients

Uses, dosage, side effects and warnings for Montelukast Sodium →

Package NDC codes (1)

Package NDCDescriptionSince
68071-5278-330 TABLET, FILM COATED in 1 BOTTLE (68071-5278-3)Jun 10, 2020

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