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Sucralfate

NDC 87063-176, Sucralfate, tablet, from ASCLEMED USA INC..

Product NDC
87063-176
Status
Listed
Labeler
ASCLEMED USA INC.
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA070848
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/87063-176 \
  -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
87063-176-0187063017601100 TABLET in 1 BOTTLE (87063-176-01)
87063-176-0587063017605500 TABLET in 1 BOTTLE (87063-176-05)
87063-176-1287063017612120 TABLET in 1 BOTTLE (87063-176-12)
87063-176-308706301763030 TABLET in 1 BOTTLE (87063-176-30)
87063-176-608706301766060 TABLET in 1 BOTTLE (87063-176-60)
87063-176-908706301769090 TABLET in 1 BOTTLE (87063-176-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/cd25eb96-29ea-48b2-bdee-c2ea98f216b8

Use it

Look up 87063-176 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/87063-176 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 87063-176. 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.