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PANTOPRAZOLE SODIUM

NDC 71610-659, PANTOPRAZOLE, tablet, delayed release, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-659
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, 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/71610-659 \
  -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
71610-659-09716100659099000 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-09)
71610-659-42716100659421800 TABLET, DELAYED RELEASE in 1 BOTTLE (71610-659-42)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c10e9c12-e39d-4b0b-bd4c-10d3e9a4cf34

Use it

Look up 71610-659 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-659 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-659. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.