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Sucralfate

NDC 68788-8779, Sucralfate, tablet, from Preferred Pharmaceuticals Inc.

Product NDC
68788-8779
Status
Listed
Labeler
Preferred Pharmaceuticals Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215705
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8779 \
  -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
68788-8779-36878887790330 TABLET in 1 BOTTLE (68788-8779-3)
68788-8779-968788877909100 TABLET in 1 BOTTLE (68788-8779-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a434bf8f-cc60-4d84-a9a4-61c3ff6b700e

Use it

Look up 68788-8779 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8779 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8779. 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.