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KRISTALOSE

NDC 66220-719, lactulose, powder, for solution, from Cumberland Pharmaceuticals Inc..

Product NDC
66220-719
Status
Listed
Labeler
Cumberland Pharmaceuticals Inc.
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074712
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/66220-719 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACTULOSE10 g/10g

Pharmacologic classes

Acidifying Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Package NDCNDC-11Package
66220-719-306622007193030 POUCH in 1 CARTON (66220-719-30) / 10 g in 1 POUCH (66220-719-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/535dd1ea-b567-49f7-9a84-8ea91e78c466

  • NADAC price for package 66220071930

    GET /v1/drugs/nadac/66220071930

Use it

Look up 66220-719 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/66220-719 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 66220-719. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.