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Sucralfate

NDC 68788-8946, Sucralfate, tablet, from Preferred Pharmaceuticals Inc..

Product NDC
68788-8946
Status
Listed
Labeler
Preferred Pharmaceuticals Inc.
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/68788-8946 \
  -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
68788-8946-168788894601100 TABLET in 1 BOTTLE (68788-8946-1)
68788-8946-36878889460330 TABLET in 1 BOTTLE (68788-8946-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5ec71444-cc55-47bd-8abc-b3cfc3b47d8e

Use it

Look up 68788-8946 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8946 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68788-8946. 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.