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Montelukast Sodium

NDC 65162-771 · Amneal Pharmaceuticals LLC

Generic nameMontelukast
Dosage formTABLET, CHEWABLE
RouteORAL
Active ingredient(s)MONTELUKAST SODIUM
Strength4 mg/1
Pharmacologic classLeukotriene Receptor Antagonist [EPC], Leukotriene Receptor Antagonists [MoA]
Marketing categoryANDA

Packages

65162-771-03 — 30 TABLET, CHEWABLE in 1 BOTTLE (65162-771-03)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62175-204 — Montelukast Sodium, 62175-205 — Montelukast Sodium, 63187-430 — Montelukast Sodium, 63187-550 — Montelukast Sodium, 63187-626 — MONTELUKAST, 63187-692 — MONTELUKAST SODIUM, 63187-751 — MONTELUKAST SODIUM, 63187-781 — Montelukast Sodium, 63187-896 — Montelukast Sodium, 65162-732 — Montelukast, 65162-772 — Montelukast, 65862-567 — Montelukast Sodium, 65862-568 — Montelukast Sodium, 65862-574 — Montelukast Sodium, 67046-2060 — Montelukast, 67296-1926 — Montelukast Sodium, 68001-361 — Montelukast, 68071-3355 — Montelukast Sodium, 68071-3855 — Montelukast, 68071-4034 — Montelukast, +61 more

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