Package 80425-0354-2

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 80425-0354-2
Digits Only 8042503542
Product NDC 80425-0354
Product ID 80425-0354_2a99a670-af29-299d-e063-6294a90a05d2
Description

60 CAPSULE, GELATIN COATED in 1 BOTTLE (80425-0354-2)

Marketing

Marketing Status
Marketed Since 2023-08-16
Brand lubiprostone
Generic lubiprostone
Sample Package No

Linked Drug Pages (1)

Lubiprostone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a99a670-af29-299d-e063-6294a90a05d2", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["794639"], "spl_set_id": ["031170a4-5f7d-b371-e063-6394a90ae21d"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (80425-0354-2)", "package_ndc": "80425-0354-2", "marketing_start_date": "20230816"}], "brand_name": "Lubiprostone", "product_id": "80425-0354_2a99a670-af29-299d-e063-6294a90a05d2", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "80425-0354", "generic_name": "lubiprostone", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "8 ug/1"}], "application_number": "NDA021908", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20230816", "listing_expiration_date": "20261231"}