Package 63629-1117-1

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1117-1
Digits Only 6362911171
Product NDC 63629-1117
Product ID 63629-1117_e3cb1ae5-2201-4bd9-9219-bd980c1584a5
Description

30 TABLET, FILM COATED in 1 BOTTLE (63629-1117-1)

Marketing

Marketing Status
Marketed Since 2016-12-05
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": "e3cb1ae5-2201-4bd9-9219-bd980c1584a5", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["c7def1b5-ed4d-4eb8-b566-08dbab830cfb"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63629-1117-1)", "package_ndc": "63629-1117-1", "marketing_start_date": "20161205"}], "brand_name": "donepezil hydrochloride", "product_id": "63629-1117_e3cb1ae5-2201-4bd9-9219-bd980c1584a5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "63629-1117", "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"}