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Pantoprazole Sodium

NDC 65862-559, Pantoprazole Sodium, tablet, delayed release, from Aurobindo Pharma Limited.

Product NDC
65862-559
Status
Listed
Labeler
Aurobindo Pharma Limited
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/65862-559 \
  -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
65862-559-106586205591010 BLISTER PACK in 1 CARTON (65862-559-10) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK
65862-559-906586205599090 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-90)
65862-559-99658620559991000 TABLET, DELAYED RELEASE in 1 BOTTLE (65862-559-99)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/7418f358-f536-4de6-adf0-562b4373f2e3

  • NADAC price for package 65862055990

    GET /v1/drugs/nadac/65862055990

Use it

Look up 65862-559 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65862-559 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65862-559. 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.