United States · FDA National Drug Code directory
Teriflunomide
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
- 70710-1115_52364a7a-fc8b-4d35-b24c-57f9cc367449
- Product NDC
- 70710-1115
- Form
- TABLET, FILM COATED
- Composition / generic term
- Teriflunomide
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230214
- Source listing expiry
- 20271231
Source-listed ingredients
- TERIFLUNOMIDE — 14 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (70710-1115-3) · 70710-1115-3
- 2 CARTON in 1 CARTON (70710-1115-8) / 1 BLISTER PACK in 1 CARTON (70710-1115-7) / 14 TABLET, FILM COATED in 1 BLISTER PACK · 70710-1115-8
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 →