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Pantoprazole Sodium

NDC 63187-938, Pantoprazole Sodium, tablet, delayed release, from Proficient Rx LP.

Product NDC
63187-938
Status
Listed
Labeler
Proficient Rx LP
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/63187-938 \
  -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
63187-938-306318709383030 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-938-30)
63187-938-606318709386060 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-938-60)
63187-938-906318709389090 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-938-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a03aa46f-9eb5-4cf4-addf-745d94af8261

Use it

Look up 63187-938 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63187-938 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63187-938. 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.