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Sucralfate

NDC 72578-081, Sucralfate, tablet, from Viona Pharmaceuticals Inc.

Product NDC
72578-081
Status
Listed
Labeler
Viona Pharmaceuticals Inc
Dosage form
TABLET
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA215705
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72578-081 \
  -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
72578-081-0172578008101100 TABLET in 1 BOTTLE (72578-081-01)
72578-081-0572578008105500 TABLET in 1 BOTTLE (72578-081-05)
72578-081-067257800810630 TABLET in 1 BOTTLE (72578-081-06)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c708201b-2618-4470-a3ff-8ecf04d6b3a0

  • NADAC price for package 72578008101

    GET /v1/drugs/nadac/72578008101

  • NADAC price for package 72578008105

    GET /v1/drugs/nadac/72578008105

Use it

Look up 72578-081 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72578-081 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72578-081. 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.