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Pantoprazole Sodium

NDC 72162-1746, Pantoprazole Sodium, tablet, delayed release, from Bryant Ranch Prepack.

Product NDC
72162-1746
Status
Listed
Labeler
Bryant Ranch Prepack
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/72162-1746 \
  -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
72162-1746-37216217460330 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-3)
72162-1746-67216217460660 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-6)
72162-1746-97216217460990 TABLET, DELAYED RELEASE in 1 BOTTLE (72162-1746-9)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3e5421ef-0875-4a04-b17d-95cca0052c83

Use it

Look up 72162-1746 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-1746 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-1746. 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.