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RIVAROXABAN

NDC 68180-709 · Lupin Pharmaceuticals, Inc.

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

68180-709-06 — 30 TABLET, FILM COATED in 1 BOTTLE (68180-709-06)

68180-709-09 — 90 TABLET, FILM COATED in 1 BOTTLE (68180-709-09)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 62332-347 — RIVAROXABAN, 62332-348 — RIVAROXABAN, 62332-683 — RIVAROXABAN, 67877-882 — Rivaroxaban, 70748-355 — rivaroxaban granule, 71610-690 — rivaroxaban, 71921-405 — rivaroxaban, 72205-416 — Rivaroxaban, 72603-890 — Rivaroxaban, 72865-321 — RIVAROXABAN, 76282-774 — 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.