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PANTOPRAZOLE SODIUM

NDC 76420-669, PANTOPRAZOLE, tablet, delayed release, from Asclemed USA, Inc..

Product NDC
76420-669
Status
Listed
Labeler
Asclemed USA, Inc.
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/76420-669 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • PANTOPRAZOLE SODIUM40 mg/1

Pharmacologic classes

Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]

Package NDCNDC-11Package
76420-669-107642006691010 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-10)
76420-669-307642006693030 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-30)
76420-669-607642006696060 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-60)
76420-669-907642006699090 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-669-90)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/ff15c4f1-8869-4422-9631-dc488e09e583

Use it

Look up 76420-669 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/76420-669 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 76420-669. 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.