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Pantoprazole Sodium

NDC 60687-725, Pantoprazole Sodium, tablet, delayed release, from American Health Packaging.

Product NDC
60687-725
Status
Listed
Labeler
American Health Packaging
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202038
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60687-725 \
  -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
60687-725-0160687072501100 BLISTER PACK in 1 CARTON (60687-725-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-725-11)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5ff3cf6c-6f0a-4374-8b80-4e1eb1df6245
  • NADAC price for package 60687072501

    GET /v1/drugs/nadac/60687072501

Use it

Look up 60687-725 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60687-725 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60687-725. 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.