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Lactulose

NDC 68999-002, Lactulose, solution, from Chartwell Governmental & Specialty RX, LLC..

Product NDC
68999-002
Status
Listed
Labeler
Chartwell Governmental & Specialty RX, LLC.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209517
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68999-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • LACTULOSE10 g/15mL

Pharmacologic classes

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

Package NDCNDC-11Package
68999-002-24689990002242 TRAY in 1 BOX (68999-002-24) / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (68999-002-51)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/887157ba-3c91-4fbf-bb12-b49c6fa4252c

Use it

Look up 68999-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68999-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68999-002. 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.