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Pantoprazole Sodium

NDC 68071-5053, Pantoprazole Sodium, tablet, delayed release, from NuCare Pharmaceuticals,Inc..

Product NDC
68071-5053
Status
Listed
Labeler
NuCare Pharmaceuticals,Inc.
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/68071-5053 \
  -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
68071-5053-66807150530660 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-5053-6)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/924a80b9-de48-90c0-e053-2995a90a00e1

Use it

Look up 68071-5053 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/68071-5053 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 68071-5053. 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.