Lubiprostone
NDC 43598-168, Lubiprostone, capsule, gelatin coated, from Dr. Reddy's Laboratories Inc..
- Product NDC
- 43598-168
- Status
- Listed
- Labeler
- Dr. Reddy's Laboratories Inc.
- Dosage form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- NDA AUTHORIZED GENERIC
- Application
- NDA021908
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/43598-168 \ -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 |
|---|---|---|
| 43598-168-60 | 43598016860 | 60 CAPSULE, GELATIN COATED in 1 BOTTLE (43598-168-60) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/006b8b6c-f0eb-4246-87da-67582984b0e4NADAC price for package 43598016860
GET /v1/drugs/nadac/43598016860
Use it
Look up 43598-168 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/43598-168 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 43598-168. 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.