Package 72603-288-01
Brand: lubiprostone
Generic: lubiprostonePackage Facts
Identity
Package NDC
72603-288-01
Digits Only
7260328801
Product NDC
72603-288
Description
60 CAPSULE in 1 BOTTLE (72603-288-01)
Marketing
Marketing Status
Brand
lubiprostone
Generic
lubiprostone
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4d72c56c-4948-4cd4-afc4-e1e0d59622a5", "openfda": {"nui": ["N0000175573", "N0000175456"], "upc": ["0372603289015", "0372603288018"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["1626ac65-ea12-421b-9780-bfdb50a39e1a"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (72603-288-01)", "package_ndc": "72603-288-01", "marketing_start_date": "20250701"}], "brand_name": "Lubiprostone", "product_id": "72603-288_4d72c56c-4948-4cd4-afc4-e1e0d59622a5", "dosage_form": "CAPSULE", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "72603-288", "generic_name": "lubiprostone", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": ".008 mg/1"}], "application_number": "ANDA218640", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}