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PANTOPRAZOLE SODIUM

NDC 42708-104, PANTOPRAZOLE, tablet, delayed release, from QPharma Inc.

Product NDC
42708-104
Status
Listed
Labeler
QPharma 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/42708-104 \
  -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
42708-104-304270801043030 TABLET, DELAYED RELEASE in 1 BOTTLE (42708-104-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b4a94a37-47c1-4dd9-9e4d-5b4a03480aa6

Use it

Look up 42708-104 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/42708-104 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 42708-104. 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.