United States · FDA National Drug Code directory
LAMPIT
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
- 50419-750_9b14492a-5ae2-4d0a-85c0-212636daf8cd
- Product NDC
- 50419-750
- Form
- TABLET, FILM COATED
- Composition / generic term
- nifurtimox
- Labeler
- Bayer HealthCare Pharmaceuticals Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20201001
- Source listing expiry
- 20271231
Source-listed ingredients
- NIFURTIMOX — 30 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (50419-750-01) / 100 TABLET, FILM COATED in 1 BOTTLE · 50419-750-01
Source and coverage
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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.
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