RIVAROXABAN

NDC 62332-346 · Alembic Pharmaceuticals Inc.

Generic nameRIVAROXABAN

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)RIVAROXABAN

Strength10 mg/1

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

Marketing categoryANDA

Packages

62332-346-10 — 100 BLISTER PACK in 1 CARTON (62332-346-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

62332-346-30 — 30 TABLET, FILM COATED in 1 BOTTLE (62332-346-30)

62332-346-90 — 90 TABLET, FILM COATED in 1 BOTTLE (62332-346-90)

62332-346-91 — 1000 TABLET, FILM COATED in 1 BOTTLE (62332-346-91)

FDA lists these products with the same active ingredient.

50458-580 — rivaroxaban, 51672-4228 — Rivaroxaban, 55154-1422 — rivaroxaban, 55154-1423 — rivaroxaban, 55154-1424 — rivaroxaban, 55488-0540 — rivaroxaban, 55488-0541 — rivaroxaban, 55488-0542 — rivaroxaban, 59651-849 — Rivaroxaban, 60505-6256 — Rivaroxaban, 62332-347 — RIVAROXABAN, 62332-348 — RIVAROXABAN, 62332-683 — RIVAROXABAN, 67877-882 — Rivaroxaban, 68180-709 — RIVAROXABAN, 70748-355 — rivaroxaban granule, 71610-690 — rivaroxaban, 71921-405 — rivaroxaban, 72205-416 — Rivaroxaban, 72603-890 — 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.