United States · FDA National Drug Code directory
Lactulose
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
- 0121-0965_78330d1b-d8d8-46ab-afcd-3a6362520db6
- Product NDC
- 0121-0965
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- Lactulose
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250317
- Source listing expiry
- 20271231
Source-listed ingredients
- LACTULOSE — 10 g/10g
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (0121-0965-30) / 10 g in 1 POUCH (0121-0965-01) · 0121-0965-30
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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