TIOPRONIN
Active substance: tiopronin
TABLET, DELAYED RELEASE · TIOPRONIN 300 mg/1
United StatesActive
Marketing holder: Par Health USA, LLC
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- TIOPRONIN · 300 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208c-bb27-7e90-a6c1-ad628708380b,01a1208d-1fee-7390-b34b-02d7204d23b9,01a1208e-4890-7152-8549-f3fb4b4155c8,01a1208e-4896-76a1-8e51-a22769f601bf,01a1208e-dfda-723c-8bfb-173fe26b0939;count=16 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 0254-3035
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 0254-3035 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 0254-3035 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 0254-3035 · Verified 2026-10-09 · open in source