NDC 68001-361 – Montelukast

Montelukast Sodium 10 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68001-361

Product details

Brand name
Montelukast
Generic name
Montelukast
Labeler
BluePoint Laboratories
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA203366
Marketed since
June 29, 2018
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
68001-361-03500 TABLET in 1 BOTTLE (68001-361-03)Jun 29, 2018
68001-361-0430 TABLET in 1 BOTTLE (68001-361-04)Jun 29, 2018
68001-361-0590 TABLET in 1 BOTTLE (68001-361-05)Jun 29, 2018

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