Package 31722-404-60

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 31722-404-60
Digits Only 3172240460
Product NDC 31722-404
Description

60 CAPSULE in 1 BOTTLE (31722-404-60)

Marketing

Marketing Status
Marketed Since 2025-05-27
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": "5008a4ec-08c5-4d06-bac9-e7239620a07d", "openfda": {"nui": ["N0000175573", "N0000175456"], "upc": ["0331722404600", "0331722403603"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["6d973d7d-a43e-4495-b618-a8ad3142683d"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE in 1 BOTTLE (31722-404-60)", "package_ndc": "31722-404-60", "marketing_start_date": "20250527"}], "brand_name": "Lubiprostone", "product_id": "31722-404_5008a4ec-08c5-4d06-bac9-e7239620a07d", "dosage_form": "CAPSULE", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "31722-404", "generic_name": "lubiprostone", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": ".024 mg/1"}], "application_number": "ANDA218640", "marketing_category": "ANDA", "marketing_start_date": "20250527", "listing_expiration_date": "20261231"}