Package 63629-1118-1

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-1118-1
Digits Only 6362911181
Product NDC 63629-1118
Product ID 63629-1118_bfa44376-0f36-4803-add3-5304205fc5f2
Description

90 TABLET, FILM COATED in 1 BOTTLE (63629-1118-1)

Marketing

Marketing Status
Marketed Since 2020-07-30
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": "bfa44376-0f36-4803-add3-5304205fc5f2", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["045529cb-0a13-41fc-96db-f9e26b7db312"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63629-1118-1)", "package_ndc": "63629-1118-1", "marketing_start_date": "20200730"}], "brand_name": "donepezil hydrochloride", "product_id": "63629-1118_bfa44376-0f36-4803-add3-5304205fc5f2", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "63629-1118", "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": "20200730", "listing_expiration_date": "20261231"}