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PANTOPRAZOLE SODIUM

NDC 64980-676, PANTOPRAZOLE SODIUM, tablet, delayed release, from Rising Pharma Holdings, Inc..

Product NDC
64980-676
Status
Listed
Labeler
Rising Pharma Holdings, Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA219087
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/64980-676 \
  -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
64980-676-096498006760990 TABLET, DELAYED RELEASE in 1 BOTTLE (64980-676-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/91a6b13f-457f-4136-9541-c4adb9c3c35c

  • NADAC price for package 64980067609

    GET /v1/drugs/nadac/64980067609

Use it

Look up 64980-676 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64980-676 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64980-676. 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.