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RIVAROXABAN

NDC 62332-347 · Alembic Pharmaceuticals Inc.

Generic nameRIVAROXABAN
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)RIVAROXABAN
Strength15 mg/1
Pharmacologic classFactor Xa Inhibitor [EPC], Factor Xa Inhibitors [MoA]
Marketing categoryANDA

Packages

62332-347-10 — 100 BLISTER PACK in 1 CARTON (62332-347-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK

62332-347-30 — 30 TABLET, FILM COATED in 1 BOTTLE (62332-347-30)

62332-347-90 — 90 TABLET, FILM COATED in 1 BOTTLE (62332-347-90)

62332-347-91 — 1000 TABLET, FILM COATED in 1 BOTTLE (62332-347-91)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 62332-346 — 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, 72865-321 — RIVAROXABAN, +23 more

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