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Montelukast

NDC 50268-556 · AvPAK

Generic nameMontelukast
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

50268-556-15 — 50 BLISTER PACK in 1 BOX (50268-556-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-556-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

29300-221 — montelukast sodium, 29300-222 — montelukast sodium, 31722-726 — MONTELUKAST SODIUM, 33342-102 — Montelukast, 42291-622 — Montelukast Sodium, 42291-623 — Montelukast Sodium, 43063-381 — Montelukast Sodium, 43063-762 — Montelukast Sodium, 50090-6108 — Montelukast, 50090-6109 — MONTELUKAST SODIUM, 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, 57237-255 — Montelukast Sodium, 59651-329 — 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.