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Lactulose

NDC 69067-020, Lactulose, solution, from Foxland Pharmaceuticals, Inc..

Product NDC
69067-020
Status
Listed
Labeler
Foxland Pharmaceuticals, Inc.
Dosage form
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/69067-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACTULOSE20 g/20g

Pharmacologic classes

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

Package NDCNDC-11Package
69067-020-156906700201515 PACKET in 1 CARTON (69067-020-15) / 20 g in 1 PACKET

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3363bdbd-f0d1-45b3-8193-7fdb0a310cc2

Use it

Look up 69067-020 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69067-020 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69067-020. 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.