Pantoprazole Sodium DR
NDC 80425-0085, Pantoprazole Sodium, tablet, delayed release, from Advanced Rx of Tennessee, LLC.
- Product NDC
- 80425-0085
- Status
- Listed
- Labeler
- Advanced Rx of Tennessee, LLC
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA205119
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0085 \ -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 NDC | NDC-11 | Package |
|---|---|---|
| 80425-0085-3 | 80425008503 | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0085-3) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b3277cb8-26d0-bce0-e053-2a95a90af6dd
Use it
Look up 80425-0085 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0085 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 80425-0085. 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.