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Montelukast

NDC 68001-361 · BluePoint Laboratories

Generic nameMontelukast
Dosage formTABLET
RouteORAL
Active ingredient(s)MONTELUKAST SODIUM
Strength10 mg/1
Pharmacologic classLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

68001-361-03 — 500 TABLET in 1 BOTTLE (68001-361-03)

68001-361-04 — 30 TABLET in 1 BOTTLE (68001-361-04)

68001-361-05 — 90 TABLET in 1 BOTTLE (68001-361-05)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63187-781 — Montelukast Sodium, 63187-896 — Montelukast Sodium, 65162-732 — Montelukast, 65162-771 — Montelukast, 65162-772 — Montelukast, 65862-567 — Montelukast Sodium, 65862-568 — Montelukast Sodium, 65862-574 — Montelukast Sodium, 67046-2060 — Montelukast, 67296-1926 — Montelukast Sodium, 68071-3355 — Montelukast Sodium, 68071-3855 — Montelukast, 68071-4034 — Montelukast, 68071-4047 — Montelukast Sodium, 68071-5278 — montelukast sodium, 68084-875 — Montelukast Sodium, 68788-8099 — Montelukast, 68788-8610 — Montelukast Sodium, 68788-8617 — montelukast sodium, 69367-287 — Montelukast Sodium, +61 more

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