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Pantoprazole Sodium DR

NDC 80425-0406, Pantoprazole Sodium, tablet, delayed release, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0406
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202038
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0406 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM20 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
80425-0406-18042504060130 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-1)
80425-0406-28042504060260 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-2)
80425-0406-38042504060390 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0406-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1c46140c-2399-5ca3-e063-6394a90af33b

Use it

Look up 80425-0406 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0406 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0406. 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.