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pantoprazole sodium

NDC 70010-191, pantoprazole sodium, tablet, delayed release, from Granules Pharmaceuticals Inc..

Product NDC
70010-191
Status
Listed
Labeler
Granules Pharmaceuticals Inc.
Dosage form
TABLET, DELAYED RELEASE
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217282
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70010-191 \
  -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
70010-191-097001001910990 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-191-09)
70010-191-10700100191101000 TABLET, DELAYED RELEASE in 1 BOTTLE (70010-191-10)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8f2fb647-15bc-41cb-84a4-02e956e614fc

  • NADAC price for package 70010019109

    GET /v1/drugs/nadac/70010019109

  • NADAC price for package 70010019110

    GET /v1/drugs/nadac/70010019110

Use it

Look up 70010-191 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70010-191 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70010-191. 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.