United States · FDA National Drug Code directory
XARELTO
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 50458-577_5294926b-7812-41da-a0e8-56f492198450
- Product NDC
- 50458-577
- Form
- TABLET, FILM COATED
- Composition / generic term
- rivaroxaban
- Labeler
- Janssen Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20181009
- Source listing expiry
- 20271231
Source-listed ingredients
- RIVAROXABAN — 2.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 BLISTER PACK in 1 BOX, UNIT-DOSE (50458-577-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK (50458-577-01) · 50458-577-10
- 14 TABLET, FILM COATED in 1 BOTTLE (50458-577-14) · 50458-577-14
- 180 TABLET, FILM COATED in 1 BOTTLE (50458-577-18) · 50458-577-18
- 60 TABLET, FILM COATED in 1 BOTTLE (50458-577-60) · 50458-577-60
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →