Package 72162-2137-5

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-2137-5
Digits Only 7216221375
Product NDC 72162-2137
Description

500 TABLET in 1 BOTTLE (72162-2137-5)

Marketing

Marketing Status
Marketed Since 2021-06-29
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": "693b7fb1-3c85-456b-98ae-67df323703ee", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["7ab9d0ef-e30c-46e9-9911-435a7b65c47b"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (72162-2137-0)", "package_ndc": "72162-2137-0", "marketing_start_date": "20210629"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (72162-2137-3)", "package_ndc": "72162-2137-3", "marketing_start_date": "20210629"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2137-5)", "package_ndc": "72162-2137-5", "marketing_start_date": "20210629"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (72162-2137-9)", "package_ndc": "72162-2137-9", "marketing_start_date": "20210629"}], "brand_name": "Donepezil Hydrochloride", "product_id": "72162-2137_693b7fb1-3c85-456b-98ae-67df323703ee", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72162-2137", "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": "10 mg/1"}], "application_number": "ANDA078662", "marketing_category": "ANDA", "marketing_start_date": "20210629", "listing_expiration_date": "20261231"}