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LACTULOSE

NDC 17856-0874, Lactulose, solution, from Atlantic Biologicals Corp..

Product NDC
17856-0874
Status
Listed
Labeler
Atlantic Biologicals Corp.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074623
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0874 \
  -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
17856-0874-31785608740350 CUP, UNIT-DOSE in 1 CASE (17856-0874-3) / 30 mL in 1 CUP, UNIT-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3fb6e908-893c-5a57-e063-6294a90a1bfc

Use it

Look up 17856-0874 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0874 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-0874. 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.