Lubiprostone 63304-0352
Product NDC
63304-0352- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule, Gelatin Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 1, 2023
- 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 (63304-352-60)