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
- 68999-002_437b8b21-3264-1b6c-e063-6294a90a1d51
- Product NDC
- 68999-002
- Form
- SOLUTION
- Composition / generic term
- Lactulose
- Labeler
- Chartwell Governmental & Specialty RX, LLC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20181123
- Source listing expiry
- 20261231
Source-listed ingredients
- LACTULOSE — 10 g/15mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 TRAY in 1 BOX (68999-002-24) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (68999-002-51) · 68999-002-24
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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