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Protonix I.V.

NDC 0008-4001, PANTOPRAZOLE SODIUM, injection, powder, for solution, from Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..

Product NDC
0008-4001
Status
Listed
Labeler
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Dosage form
INJECTION, POWDER, FOR SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA020988
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0008-4001 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM40 mg/10mL

Pharmacologic classes

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

Package NDCNDC-11Package
0008-4001-100000840011010 CARTON in 1 PACKAGE (0008-4001-10) / 1 VIAL in 1 CARTON (0008-4001-01) / 10 mL in 1 VIAL
0008-4001-250000840012525 CARTON in 1 PACKAGE (0008-4001-25) / 1 VIAL in 1 CARTON (0008-4001-01) / 10 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f39b3e7d-39d2-4c8a-9974-4ab885241880

Use it

Look up 0008-4001 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0008-4001 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0008-4001. 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.