Rivaroxaban

NDC 33342-488 · Macleods Pharmaceuticals Limited

Generic nameRivaroxaban

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)RIVAROXABAN

Strength2.5 mg/1

Pharmacologic classFactor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]

Marketing categoryANDA

Packages

33342-488-09 — 60 TABLET, FILM COATED in 1 BOTTLE (33342-488-09)

33342-488-57 — 180 TABLET, FILM COATED in 1 BOTTLE (33342-488-57)

33342-488-98 — 10 BLISTER PACK in 1 CARTON (33342-488-98) / 6 TABLET, FILM COATED in 1 BLISTER PACK

FDA lists these products with the same active ingredient.

14445-147 — Rivaroxaban, 14445-148 — Rivaroxaban, 14445-183 — Rivaroxaban, 14445-184 — Rivaroxaban, 31722-496 — RIVAROXABAN, 42571-345 — RIVAROXABAN, 43598-981 — Rivaroxaban, 46708-346 — RIVAROXABAN, 46708-347 — RIVAROXABAN, 46708-348 — RIVAROXABAN, 46708-683 — RIVAROXABAN, 50090-3625 — rivaroxaban, 50090-3639 — rivaroxaban, 50090-4468 — rivaroxaban, 50090-4469 — rivaroxaban, 50228-513 — Rivaroxaban, 50458-575 — rivaroxaban, 50458-577 — rivaroxaban, 50458-578 — rivaroxaban, 50458-579 — rivaroxaban, +23 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.