Package 0480-3479-06
Brand: lubiprostone
Generic: lubiprostonePackage Facts
Identity
Package NDC
0480-3479-06
Digits Only
0480347906
Product NDC
0480-3479
Description
60 CAPSULE, GELATIN COATED in 1 BOTTLE (0480-3479-06)
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": "22f53da2-2fb9-411d-baad-fef011383f6f", "openfda": {"nui": ["N0000175573", "N0000175456"], "upc": ["0304804138069", "0304803479064"], "unii": ["7662KG2R6K"], "rxcui": ["616578", "794639"], "spl_set_id": ["e17b521e-2c25-4bef-82f9-7916fa79bca4"], "pharm_class_epc": ["Chloride Channel Activator [EPC]"], "pharm_class_moa": ["Chloride Channel Activators [MoA]"], "manufacturer_name": ["Teva Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 CAPSULE, GELATIN COATED in 1 BOTTLE (0480-3479-06)", "package_ndc": "0480-3479-06", "marketing_start_date": "20230103"}], "brand_name": "Lubiprostone", "product_id": "0480-3479_22f53da2-2fb9-411d-baad-fef011383f6f", "dosage_form": "CAPSULE, GELATIN COATED", "pharm_class": ["Chloride Channel Activator [EPC]", "Chloride Channel Activators [MoA]"], "product_ndc": "0480-3479", "generic_name": "Lubiprostone", "labeler_name": "Teva Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lubiprostone", "active_ingredients": [{"name": "LUBIPROSTONE", "strength": "8 ug/1"}], "application_number": "ANDA209920", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}