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Sucralfate

NDC 80425-0091, Sucralfate, tablet, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0091
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070848
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0091 \
  -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
80425-0091-18042500910130 TABLET in 1 BOTTLE (80425-0091-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b39f22c8-f224-451a-e053-2995a90aaad7

Use it

Look up 80425-0091 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0091 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0091. 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.