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
- 51672-4243_3b8ff35a-8b5e-7aca-e063-6394a90aea34
- Product NDC
- 51672-4243
- Form
- SOLUTION
- Composition / generic term
- Lactulose
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250602
- Source listing expiry
- 20261231
Source-listed ingredients
- LACTULOSE — 10 g/15mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (51672-4243-9) / 473 mL in 1 BOTTLE · 51672-4243-9
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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