Package 72189-607-60

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 72189-607-60
Digits Only 7218960760
Product NDC 72189-607
Product ID 72189-607_2bd6f613-64d1-0291-e063-6294a90a0238
Description

60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)

Marketing

Marketing Status
Marketed Since 2025-01-16
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": "2bd6f613-64d1-0291-e063-6294a90a0238", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["616578"], "spl_set_id": ["2bd6f613-64d0-0291-e063-6294a90a0238"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Direct Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (72189-607-60)", "package_ndc": "72189-607-60", "marketing_start_date": "20250116"}], "brand_name": "Lubiprostone", "product_id": "72189-607_2bd6f613-64d1-0291-e063-6294a90a0238", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "72189-607", "generic_name": "Lubiprostone", "labeler_name": "Direct Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "24 ug/1"}], "application_number": "NDA021908", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20250116", "listing_expiration_date": "20261231"}