Lubiprostone 72189-0607
Product NDC
72189-0607- Manufacturer
- Direct Rx
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 16, 2025
- Listing Expires
- December 31, 2026
- Application
- NDA021908
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Lubiprostone | 24 ug/1 |
Drug Class
Chloride Channel Activator [EPC]Chloride Channel Activator [EPC]Chloride Channel Activators [MoA]
Packaging Options(1)
60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)