United States · FDA National Drug Code directory
RIVAROXABAN
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
- 46708-683_4b61dc52-0593-4ef0-8246-a82ff6972842
- Product NDC
- 46708-683
- Form
- TABLET, FILM COATED
- Composition / generic term
- RIVAROXABAN
- Labeler
- Alembic Pharmaceuticals Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250514
- Source listing expiry
- 20261231
Source-listed ingredients
- RIVAROXABAN — 2.5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 BLISTER PACK in 1 CARTON (46708-683-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 46708-683-10
- 180 TABLET, FILM COATED in 1 BOTTLE (46708-683-45) · 46708-683-45
- 60 TABLET, FILM COATED in 1 BOTTLE (46708-683-60) · 46708-683-60
- 1000 TABLET, FILM COATED in 1 BOTTLE (46708-683-91) · 46708-683-91
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 →