Skip to main content

montelukast sodium

NDC 68788-7669 · Preferred Pharmaceuticals, Inc.

Generic namemontelukast sodium
Dosage formTABLET, CHEWABLE
RouteORAL
Active ingredient(s)MONTELUKAST
Strength5 mg/1
Pharmacologic classLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

68788-7669-1 — 10 TABLET, CHEWABLE in 1 BOTTLE (68788-7669-1)

68788-7669-2 — 20 TABLET, CHEWABLE in 1 BOTTLE (68788-7669-2)

68788-7669-3 — 30 TABLET, CHEWABLE in 1 BOTTLE (68788-7669-3)

68788-7669-4 — 14 TABLET, CHEWABLE in 1 BOTTLE (68788-7669-4)

68788-7669-6 — 60 TABLET, CHEWABLE in 1 BOTTLE (68788-7669-6)

68788-7669-9 — 90 TABLET, CHEWABLE in 1 BOTTLE (68788-7669-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

31722-727 — montelukast sodium, 31722-728 — montelukast sodium, 33342-110 — Montelukast sodium, 33342-111 — Montelukast sodium, 50090-2921 — montelukast sodium, 50090-4705 — montelukast sodium, 50090-7920 — montelukast sodium, 50090-7925 — montelukast sodium, 72189-223 — MONTELUKAST SODIUM

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.