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Sucralfate

NDC 69238-1656, Sucralfate, tablet, from Amneal Pharmaceuticals NY LLC.

Product NDC
69238-1656
Status
Listed
Labeler
Amneal Pharmaceuticals NY LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215576
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1656 \
  -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
69238-1656-169238165601100 TABLET in 1 BOTTLE (69238-1656-1)
69238-1656-569238165605500 TABLET in 1 BOTTLE (69238-1656-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a4f722e7-2885-4f27-8358-9c662439600a

  • NADAC price for package 69238165601

    GET /v1/drugs/nadac/69238165601

Use it

Look up 69238-1656 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-1656 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69238-1656. 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.