Package 63629-8483-1

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8483-1
Digits Only 6362984831
Product NDC 63629-8483
Product ID 63629-8483_6f78fe1c-7057-41ef-bea2-4f932a842178
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-8483-1)

Marketing

Marketing Status
Marketed Since 2021-05-18
Brand donepezil hydrochloride
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (1)

Donepezil Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "6f78fe1c-7057-41ef-bea2-4f932a842178", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["caebc31c-5a35-4434-b7e2-80f6405383ca"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-8483-1)", "package_ndc": "63629-8483-1", "marketing_start_date": "20210518"}], "brand_name": "Donepezil Hydrochloride", "product_id": "63629-8483_6f78fe1c-7057-41ef-bea2-4f932a842178", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "63629-8483", "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": "ANDA203104", "marketing_category": "ANDA", "marketing_start_date": "20150301", "listing_expiration_date": "20261231"}