RABEPRAZOLE SODIUM
NDC 68788-8536, rabeprazole sodium, tablet, delayed release, from Preferred Pharmaceuticals Inc..
- Product NDC
- 68788-8536
- Status
- Listed
- Labeler
- Preferred Pharmaceuticals Inc.
- Dosage form
- TABLET, DELAYED RELEASE
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA204237
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8536 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- RABEPRAZOLE SODIUM20 mg/1
Pharmacologic classes
Proton Pump Inhibitor [EPC]; Proton Pump Inhibitors [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 68788-8536-3 | 68788853603 | 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8536-3) |
| 68788-8536-6 | 68788853606 | 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8536-6) |
Linked data
RxNorm, label and prices
Related lookups
FDA label sections
GET /v1/drugs/labels/4582d443-f1be-4f94-85da-49aa603f54e4
Use it
Look up 68788-8536 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/68788-8536 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 68788-8536. 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.