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Lactulose

NDC 0121-0965, Lactulose, powder, for solution, from PAI Holdings, LLC dba PAI Pharma.

Product NDC
0121-0965
Status
Listed
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
POWDER, FOR SOLUTION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217914
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0965 \
  -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
0121-0965-300012109653030 POUCH in 1 CARTON (0121-0965-30) / 10 g in 1 POUCH (0121-0965-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5ae4b6da-44df-419a-9f2b-8c4d79f635c8

  • NADAC price for package 00121096530

    GET /v1/drugs/nadac/00121096530

Use it

Look up 0121-0965 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0121-0965 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0121-0965. 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.