Package 83008-001-60

Brand: lubiprostone

Generic: lubiprostone
NDC Package

Package Facts

Identity

Package NDC 83008-001-60
Digits Only 8300800160
Product NDC 83008-001
Description

60 CAPSULE, GELATIN COATED in 1 BOTTLE (83008-001-60)

Marketing

Marketing Status
Discontinued 2026-08-31
Brand lubiprostone
Generic lubiprostone
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fd3c99bd-7841-472f-bb74-abe1dc15ee8a", "openfda": {"nui": ["N0000175573", "N0000175456"], "unii": ["7662KG2R6K"], "rxcui": ["616578"], "spl_set_id": ["9bffe7c4-40f2-4490-a32f-15d525000928"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (83008-001-60)", "package_ndc": "83008-001-60", "marketing_end_date": "20260831", "marketing_start_date": "20230314"}], "brand_name": "Lubiprostone", "product_id": "83008-001_fd3c99bd-7841-472f-bb74-abe1dc15ee8a", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "83008-001", "generic_name": "lubiprostone", "labeler_name": "Quality Care Products, LLC", "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_end_date": "20260831", "marketing_start_date": "20230314"}