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Lactulose

NDC 51672-4243, Lactulose, solution, from Sun Pharmaceutical Industries, Inc..

Product NDC
51672-4243
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218858
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4243 \
  -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
51672-4243-9516724243091 BOTTLE in 1 CARTON (51672-4243-9) / 473 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/391cfd01-c1fa-41f9-abd7-d0abe9a27634

  • NADAC price for package 51672424309

    GET /v1/drugs/nadac/51672424309

Use it

Look up 51672-4243 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51672-4243 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51672-4243. 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.