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
- 69067-020_4618824a-2b40-3d54-e063-6394a90a4b96
- Product NDC
- 69067-020
- Form
- SOLUTION
- Composition / generic term
- Lactulose
- Labeler
- Foxland Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250207
- Source listing expiry
- 20261231
Source-listed ingredients
- LACTULOSE — 20 g/20g
These values do not establish equivalence or a dose recommendation.
Packages
- 15 PACKET in 1 CARTON (69067-020-15) / 20 g in 1 PACKET · 69067-020-15
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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