United States · FDA National Drug Code directory
Humatin
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
- 80725-250_4b33337a-4e4b-42f3-923f-5b61f02fc463
- Product NDC
- 80725-250
- Form
- CAPSULE
- Composition / generic term
- PAROMOMYCIN SULFATE
- Labeler
- Waylis Therapeutics LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210408
- Source listing expiry
- 20261231
Source-listed ingredients
- PAROMOMYCIN SULFATE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE in 1 BOTTLE (80725-250-01) · 80725-250-01
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 →