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Pantoprazole Sodium

NDC 65162-636, Pantoprazole, tablet, delayed release, from Amneal Pharmaceuticals LLC.

Product NDC
65162-636
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA205119
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65162-636 \
  -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
65162-636-036516206360330 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-636-03)
65162-636-096516206360990 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-636-09)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f3ded82a-cf0d-4844-944a-75f9f9215ff0

  • NADAC price for package 65162063609

    GET /v1/drugs/nadac/65162063609

Use it

Look up 65162-636 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65162-636 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65162-636. 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.