Pantoprazole Sodium
NDC 0904-6870, Pantoprazole Sodium, tablet, delayed release, from Major Pharmaceuticals.
- Product NDC
- 0904-6870
- Status
- Listed
- Labeler
- Major Pharmaceuticals
- 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/0904-6870 \ -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 |
|---|---|---|
| 0904-6870-45 | 00904687045 | 80 BLISTER PACK in 1 CARTON (0904-6870-45) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/de419aa0-caa9-40fb-bc6d-e341c94273c7NADAC price for package 00904687045
GET /v1/drugs/nadac/00904687045
Use it
Look up 0904-6870 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/0904-6870 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 0904-6870. 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.