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Sucralfate

NDC 71610-541, Sucralfate, tablet, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-541
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA074415
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71610-541 \
  -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
71610-541-607161005416090 TABLET in 1 BOTTLE, PLASTIC (71610-541-60)
71610-541-7071610054170120 TABLET in 1 BOTTLE, PLASTIC (71610-541-70)
71610-541-9471610054194360 TABLET in 1 BOTTLE, PLASTIC (71610-541-94)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b414dc07-681c-4fde-965f-09df64c015e7

Use it

Look up 71610-541 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-541 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-541. 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.