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: 73352-905_3eaf2342-fb58-e0a5-e063-6394a90a7271
Product NDC: 73352-905
Form: POWDER, FOR SOLUTION
Composition / generic term: Lactulose
Labeler: Trifluent Pharma, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20250913
Source listing expiry: 20261231

Source-listed ingredients

LACTULOSE — 20 g/20g

These values do not establish equivalence or a dose recommendation.

Packages

15 POUCH in 1 CARTON (73352-905-15) / 20 g in 1 POUCH (73352-905-01) · 73352-905-15

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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