NDC 80425-0354-2
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 Advanced Rx of Tennessee, LLC.
Key Facts
- Brand Name
- Lubiprostone
- Generic Name
- lubiprostone
- NDC Code (Package)
80425-0354-2- NDC Code (Product)
80425-0354- Manufacturer
- Advanced Rx of Tennessee, LLC
- Strength
- 8 ug/1
- Dosage Form
- CAPSULE, GELATIN COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA021908
- Drug Class
- Chloride Channel Activator [EPC]
- Marketing Start
- 08/16/2023
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.