NDC 69339-162-17
LUBIPROSTONE 8 ug/1
LUBIPROSTONE · CAPSULE, GELATIN COATED
LUBIPROSTONE is a capsule, gelatin coated containing lubiprostone at a strength of 8 ug/1. Manufactured by Natco Pharma USA LLC.
Key Facts
- Brand Name
- LUBIPROSTONE
- Generic Name
- LUBIPROSTONE
- NDC Code (Package)
69339-162-17- NDC Code (Product)
69339-162- Manufacturer
- Natco Pharma USA LLC
- Strength
- 8 ug/1
- Dosage Form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA021908
- Drug Class
- Chloride Channel Activator [EPC]
- Marketing Start
- 10/17/2022
Recall History
No Recall HistoryView Full Drug Page
LUBIPROSTONE — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.