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PANTOPRAZOLE SODIUM

NDC 82009-010, PANTOPRAZOLE, tablet, delayed release, from Quallent Pharmaceuticals Health LLC.

Product NDC
82009-010
Status
Listed
Labeler
Quallent Pharmaceuticals Health LLC
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/82009-010 \
  -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
82009-010-908200900109090 TABLET, DELAYED RELEASE in 1 BOTTLE (82009-010-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/643eb498-d916-4fb7-9281-32895575ab36

  • NADAC price for package 82009001090

    GET /v1/drugs/nadac/82009001090

Use it

Look up 82009-010 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/82009-010 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 82009-010. 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.