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
- 0527-5125_1b869904-b3c5-4f81-a333-1f26b6b2c7bf
- Product NDC
- 0527-5125
- Form
- SOLUTION
- Composition / generic term
- LACTULOSE
- Labeler
- Lannett Company, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010726
- Source listing expiry
- 20261231
Source-listed ingredients
- LACTULOSE — 10 g/15mL
These values do not establish equivalence or a dose recommendation.
Packages
- 237 mL in 1 BOTTLE (0527-5125-68) · 0527-5125-68
- 473 mL in 1 BOTTLE (0527-5125-70) · 0527-5125-70
- 946 mL in 1 BOTTLE (0527-5125-78) · 0527-5125-78
- 1892 mL in 1 BOTTLE (0527-5125-82) · 0527-5125-82
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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