Pantoprazole Sodium
NDC 35573-428, Pantoprazole Sodium, tablet, delayed release, from Burel Pharmaceuticals, LLC.
- Product NDC
- 35573-428
- Status
- Listed
- Labeler
- Burel Pharmaceuticals, LLC
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA202038
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/35573-428 \ -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 |
|---|---|---|
| 35573-428-80 | 35573042880 | 10 BLISTER PACK in 1 CARTON (35573-428-80) / 10 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3cc5197e-6b39-4415-b963-d4bbeecd7953NADAC price for package 35573042880
GET /v1/drugs/nadac/35573042880
Use it
Look up 35573-428 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/35573-428 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 35573-428. 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.