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Sucralfate

NDC 60219-1656, Sucralfate, tablet, from Amneal Pharmaceuticals NY LLC.

Product NDC
60219-1656
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/60219-1656 \
  -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
60219-1656-160219165601100 TABLET in 1 BOTTLE (60219-1656-1)
60219-1656-560219165605500 TABLET in 1 BOTTLE (60219-1656-5)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b2e07ac7-4a8a-4b68-bb65-167d1aa86883

  • NADAC price for package 60219165601

    GET /v1/drugs/nadac/60219165601

Use it

Look up 60219-1656 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60219-1656 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60219-1656. 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.