Pantoprazole Sodium
NDC 60687-725, Pantoprazole Sodium, tablet, delayed release, from American Health Packaging.
- Product NDC
- 60687-725
- Status
- Listed
- Labeler
- American Health Packaging
- 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/60687-725 \ -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 |
|---|---|---|
| 60687-725-01 | 60687072501 | 100 BLISTER PACK in 1 CARTON (60687-725-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-725-11) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/5ff3cf6c-6f0a-4374-8b80-4e1eb1df6245NADAC price for package 60687072501
GET /v1/drugs/nadac/60687072501
Use it
Look up 60687-725 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-725 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-725. 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.