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Sucralfate

NDC 17856-0306, Sucralfate, suspension, from ATLANTIC BIOLOGICALS CORP..

Product NDC
17856-0306
Status
Listed
Labeler
ATLANTIC BIOLOGICALS CORP.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211884
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0306 \
  -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
17856-0306-11785603060172 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-0306-1) / 10 mL in 1 CUP, UNIT-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e5073597-ac51-4e7c-a9dc-7695773a01f1

Use it

Look up 17856-0306 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/17856-0306 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 17856-0306. 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.