NDC 68788-8099 – Montelukast

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

Human Prescription Drug

Product NDC68788-8099

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA202843
Marketed since
October 6, 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
68788-8099-330 TABLET, FILM COATED in 1 BOTTLE (68788-8099-3)Oct 6, 2021
68788-8099-660 TABLET, FILM COATED in 1 BOTTLE (68788-8099-6)Oct 6, 2021
68788-8099-990 TABLET, FILM COATED in 1 BOTTLE (68788-8099-9)Oct 6, 2021

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