LAMPIT
Active substance: nifurtimox
TABLET, FILM COATED · NIFURTIMOX 120 mg/1
United StatesActive
Marketing holder: Bayer HealthCare Pharmaceuticals Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- NIFURTIMOX · 120 mg/1
Import and control
Control by country
- United Statesprescription only
Source: openFDA NDC · record 01a1208d-3179-7f78-95b3-cf0d9c72a3c1,01a12096-042a-7bdc-a41d-07ecf4640691;count=2 · valid from 2026-10-09 · verified 2026-10-09
Registration
- Registration number
- 50419-751
- Registration status
- Active
- Dispensing
- Prescription only
- Route
- ORAL
Sources
- product · openFDA NDC · 50419-751 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 50419-751 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 50419-751 · Verified 2026-10-09 · open in source