Package 72162-1355-9
Brand: donepezil hydrochloride
Generic: donepezil hydrochloridePackage Facts
Identity
Package NDC
72162-1355-9
Digits Only
7216213559
Product NDC
72162-1355
Description
90 TABLET, FILM COATED in 1 BOTTLE (72162-1355-9)
Marketing
Marketing Status
Brand
donepezil hydrochloride
Generic
donepezil hydrochloride
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "71178855-2eb3-47ac-b7e5-027633986c95", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["8e63ec4f-eac9-4799-b277-ff2a396e722c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-1355-3)", "package_ndc": "72162-1355-3", "marketing_start_date": "20240201"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72162-1355-9)", "package_ndc": "72162-1355-9", "marketing_start_date": "20240201"}], "brand_name": "donepezil hydrochloride", "product_id": "72162-1355_71178855-2eb3-47ac-b7e5-027633986c95", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72162-1355", "generic_name": "donepezil hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "23 mg/1"}], "application_number": "ANDA203713", "marketing_category": "ANDA", "marketing_start_date": "20161205", "listing_expiration_date": "20261231"}