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Sucralfate

NDC 50268-745, Sucralfate Oral, suspension, from AvPAK.

Product NDC
50268-745
Status
Listed
Labeler
AvPAK
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA209356
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-745 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • SUCRALFATE1 g/10mL

Pharmacologic classes

Aluminum Complex [EPC]; Organometallic Compounds [CS]

Package NDCNDC-11Package
50268-745-145026807451440 CUP in 1 BOX (50268-745-14) / 10 mL in 1 CUP (50268-745-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e78ef7d4-faa7-aebf-e053-2995a90a6f84

Use it

Look up 50268-745 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-745 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-745. 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.