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Protonix Delayed-Release

NDC 0008-0841, PANTOPRAZOLE SODIUM, tablet, delayed release, from Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..

Product NDC
0008-0841
Status
Listed
Labeler
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020987
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0008-0841 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM40 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
0008-0841-810000808418190 TABLET, DELAYED RELEASE in 1 BOTTLE (0008-0841-81)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/08098cb2-c048-4640-f387-6beec4a38936

  • NADAC price for package 00008084181

    GET /v1/drugs/nadac/00008084181

Use it

Look up 0008-0841 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0008-0841 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0008-0841. 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.