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Montelukast Sodium

NDC 57237-255 · Rising Pharma Holdings, Inc.

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

Packages

57237-255-30 — 30 TABLET, FILM COATED in 1 BOTTLE (57237-255-30)

57237-255-90 — 90 TABLET, FILM COATED in 1 BOTTLE (57237-255-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-6109 — MONTELUKAST SODIUM, 50268-556 — Montelukast, 50268-573 — Montelukast Sodium, 50268-574 — Montelukast Sodium, 55111-593 — Montelukast Sodium, 55111-594 — Montelukast Sodium, 55111-725 — Montelukast Sodium, 55154-8075 — Montelukast Sodium, 57237-212 — Montelukast Sodium, 57237-213 — Montelukast Sodium, 59651-329 — Montelukast Sodium, 62135-781 — MONTELUKAST SODIUM, 62135-782 — MONTELUKAST SODIUM, 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, +61 more

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