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Pantoprazole Sodium

NDC 50268-639, Pantoprazole Sodium, tablet, delayed release, from AvPAK.

Product NDC
50268-639
Status
Listed
Labeler
AvPAK
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078281
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/50268-639 \
  -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
50268-639-155026806391550 BLISTER PACK in 1 BOX (50268-639-15) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-639-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dcac4022-fea1-67c5-3331-fefcc3c440d8

  • NADAC price for package 50268063915

    GET /v1/drugs/nadac/50268063915

Use it

Look up 50268-639 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/50268-639 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 50268-639. 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.