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
0121-1930_78330d1b-d8d8-46ab-afcd-3a6362520db6
Product NDC
0121-1930
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 — 20 g/20g

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 POUCH in 1 CARTON (0121-1930-30) / 20 g in 1 POUCH (0121-1930-01) · 0121-1930-30

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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