PANTOPRAZOLE SODIUM
NDC 59651-671, PANTOPRAZOLE SODIUM, granule, delayed release, from Aurobindo Pharma Limited.
- Product NDC
- 59651-671
- Status
- Listed
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- GRANULE, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA217923
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/59651-671 \ -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 |
|---|---|---|
| 59651-671-30 | 59651067130 | 30 PACKET in 1 CARTON (59651-671-30) / 1 GRANULE, DELAYED RELEASE in 1 PACKET |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/b3cec41e-e98b-470a-8ba2-c31537023989NADAC price for package 59651067130
GET /v1/drugs/nadac/59651067130
Use it
Look up 59651-671 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/59651-671 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 59651-671. 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.