Package 82625-8802-2
Brand: movantik
Generic: naloxegol oxalatePackage Facts
Identity
Package NDC
82625-8802-2
Digits Only
8262588022
Product NDC
82625-8802
Description
90 TABLET, FILM COATED in 1 BOTTLE (82625-8802-2)
Marketing
Marketing Status
Brand
movantik
Generic
naloxegol oxalate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6747ab38-787e-4cd4-9626-b79b0432bc36", "openfda": {"upc": ["0382625880213", "0382625880114"], "unii": ["65I14TNM33"], "rxcui": ["1551782", "1551917", "1551923", "1601373"], "spl_set_id": ["28596788-b73f-4247-85fc-3105f51fff5a"], "manufacturer_name": ["Valinor Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (82625-8802-1)", "package_ndc": "82625-8802-1", "marketing_start_date": "20230328"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (82625-8802-2)", "package_ndc": "82625-8802-2", "marketing_start_date": "20230328"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (82625-8802-3) / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "82625-8802-3", "marketing_start_date": "20230328"}, {"sample": true, "description": "1 BLISTER PACK in 1 CARTON (82625-8802-4) / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "82625-8802-4", "marketing_start_date": "20230328"}], "brand_name": "MOVANTIK", "product_id": "82625-8802_6747ab38-787e-4cd4-9626-b79b0432bc36", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Opioid Antagonist [EPC]", "Opioid Antagonists [MoA]"], "product_ndc": "82625-8802", "generic_name": "naloxegol oxalate", "labeler_name": "Valinor Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "MOVANTIK", "active_ingredients": [{"name": "NALOXEGOL OXALATE", "strength": "25 mg/1"}], "application_number": "NDA204760", "marketing_category": "NDA", "marketing_start_date": "20230328", "listing_expiration_date": "20261231"}