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PANTOPRAZOLE SODIUM

NDC 63187-831, PANTOPRAZOLE, tablet, delayed release, from Proficient Rx LP.

Product NDC
63187-831
Status
Listed
Labeler
Proficient Rx LP
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202882
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/63187-831 \
  -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
63187-831-306318708313030 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-30)
63187-831-606318708316060 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-60)
63187-831-906318708319090 TABLET, DELAYED RELEASE in 1 BOTTLE (63187-831-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/dce2e97a-cd92-46b9-9444-91739bdcd526

Use it

Look up 63187-831 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63187-831 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63187-831. 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.