Pantoprazole Sodium
NDC 42799-952, Pantoprazole Sodium, granule, delayed release, from Edenbridge Pharmaceuticals LLC..
- Product NDC
- 42799-952
- Status
- Listed
- Labeler
- Edenbridge Pharmaceuticals LLC.
- Dosage form
- GRANULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA216247
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/42799-952 \ -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 |
|---|---|---|
| 42799-952-30 | 42799095230 | 30 PACKET in 1 CARTON (42799-952-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET (42799-952-01) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/a0bb76bc-094a-4d61-9bb2-2226c9da4ae9NADAC price for package 42799095230
GET /v1/drugs/nadac/42799095230
Use it
Look up 42799-952 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/42799-952 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 42799-952. 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.