PANTOPRAZOLE SODIUM
NDC 50268-727, PANTOPRAZOLE, tablet, delayed release, from AvPAK.
- Product NDC
- 50268-727
- Status
- Listed
- Labeler
- AvPAK
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202882
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/50268-727 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 50268-727-10 | 50268072710 | 100 BLISTER PACK in 1 BOX (50268-727-10) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (50268-727-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/59f50bcb-85e5-e3f6-e063-6294a90a11ae
Use it
Look up 50268-727 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/50268-727 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 50268-727. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.