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Pantoprazole Sodium

NDC 62175-618, Pantoprazole Sodium, tablet, delayed release, from Lannett Company, Inc..

Product NDC
62175-618
Status
Listed
Labeler
Lannett Company, Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA078281
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/62175-618 \
  -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
62175-618-43621750618431000 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-43)
62175-618-466217506184690 TABLET, DELAYED RELEASE in 1 BOTTLE (62175-618-46)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e7705bf6-e473-4b9c-bb5d-57e26ffe7b97

  • NADAC price for package 62175061846

    GET /v1/drugs/nadac/62175061846

Use it

Look up 62175-618 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/62175-618 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 62175-618. 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.