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Sucralfate

NDC 82182-106, Sucralfate, suspension, from Pacific Pharma, Inc..

Product NDC
82182-106
Status
Listed
Labeler
Pacific Pharma, Inc.
Dosage form
SUSPENSION
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA AUTHORIZED GENERIC
Application
NDA019183
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/82182-106 \
  -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
82182-106-1482182010614420 mL in 1 BOTTLE (82182-106-14)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7407c58e-766f-4e93-a1bb-c77892ae0174

  • NADAC price for package 82182010614

    GET /v1/drugs/nadac/82182010614

Use it

Look up 82182-106 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82182-106 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82182-106. 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.