United States · FDA National Drug Code directory
KRISTALOSE
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
- 66220-719_85528d56-e38f-4565-9136-c7639b479634
- Product NDC
- 66220-719
- Form
- POWDER, FOR SOLUTION
- Composition / generic term
- lactulose
- Labeler
- Cumberland Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120120
- Source listing expiry
- 20261231
Source-listed ingredients
- LACTULOSE — 10 g/10g
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (66220-719-30) / 10 g in 1 POUCH (66220-719-01) · 66220-719-30
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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