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Carafate

NDC 58914-171, Sucralfate, tablet, from Allergan, Inc..

Product NDC
58914-171
Status
Listed
Labeler
Allergan, Inc.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA018333
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/58914-171 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUCRALFATE1 g/1

Pharmacologic classes

Aluminum Complex [EPC]; Organometallic Compounds [CS]

Package NDCNDC-11Package
58914-171-1058914017110100 TABLET in 1 BOTTLE (58914-171-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c87c6b50-6977-4fa7-ae98-40c0753f7aee
  • NADAC price for package 58914017110

    GET /v1/drugs/nadac/58914017110

Use it

Look up 58914-171 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/58914-171 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 58914-171. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.