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Pantoprazole Sodium

NDC 51655-075, Pantoprazole Sodium, tablet, delayed release, from Northwind Health Company, LLC.

Product NDC
51655-075
Status
Listed
Labeler
Northwind Health Company, LLC
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/51655-075 \
  -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
51655-075-255165500752560 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-25)
51655-075-525165500755230 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51655-075-52)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f2a1af50-a051-3e55-e053-2a95a90a9184

Use it

Look up 51655-075 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51655-075 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51655-075. 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.