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Sucralfate

NDC 54738-005, Sucralfate, suspension, from Richmond Pharmaceuticals, Inc..

Product NDC
54738-005
Status
Listed
Labeler
Richmond Pharmaceuticals, Inc.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216726
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/54738-005 \
  -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
54738-005-4254738000542420 mL in 1 BOTTLE (54738-005-42)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7ac10c3f-9d50-4702-900c-41075ac6f896

Use it

Look up 54738-005 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/54738-005 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 54738-005. 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.