Lubiprostone
NDC 60687-827, Lubiprostone, capsule, gelatin coated, from American Health Packaging.
- Product NDC
- 60687-827
- Status
- Listed
- Labeler
- American Health Packaging
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA209920
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/60687-827 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- LUBIPROSTONE24 ug/1
Pharmacologic classes
Chloride Channel Activator [EPC]; Chloride Channel Activators [MoA]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 60687-827-32 | 60687082732 | 20 BLISTER PACK in 1 CARTON (60687-827-32) / 1 CAPSULE, GELATIN COATED in 1 BLISTER PACK (60687-827-33) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/3014dd6d-9c05-479d-b79d-7a49f78a1ce5NADAC price for package 60687082732
GET /v1/drugs/nadac/60687082732
Use it
Look up 60687-827 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/60687-827 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 60687-827. 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.