Package 72189-265-90

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72189-265-90
Digits Only 7218926590
Product NDC 72189-265
Product ID 72189-265_2c290521-043d-e9df-e063-6294a90a4ed8
Description

90 TABLET, FILM COATED in 1 BOTTLE (72189-265-90)

Marketing

Marketing Status
Marketed Since 2021-09-03
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": "2c290521-043d-e9df-e063-6294a90a4ed8", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["cb1b3ed1-6e68-08e2-e053-2995a90a68c4"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72189-265-90)", "package_ndc": "72189-265-90", "marketing_start_date": "20210903"}], "brand_name": "DONEPEZIL HYDROCHLORIDE", "product_id": "72189-265_2c290521-043d-e9df-e063-6294a90a4ed8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72189-265", "generic_name": "DONEPEZIL HYDROCHLORIDE", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DONEPEZIL HYDROCHLORIDE", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20210903", "listing_expiration_date": "20261231"}