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Sucralfate

NDC 71610-017, Sucralfate, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-017
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA018333
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-017 \
  -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
71610-017-607161000176090 TABLET in 1 BOTTLE (71610-017-60)
71610-017-7071610001770120 TABLET in 1 BOTTLE (71610-017-70)
71610-017-9471610001794360 TABLET in 1 BOTTLE (71610-017-94)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/84447e21-e311-4e9f-9065-53956e90135c

Use it

Look up 71610-017 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-017 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-017. 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.