Package 72162-1276-3

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72162-1276-3
Digits Only 7216212763
Product NDC 72162-1276
Product ID 72162-1276_eac36e16-c91d-4435-97dd-089068a3efaa
Description

30 TABLET, FILM COATED in 1 BOTTLE (72162-1276-3)

Marketing

Marketing Status
Marketed Since 2024-02-05
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": "eac36e16-c91d-4435-97dd-089068a3efaa", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["8090bff0-e0f0-4846-a2ab-cb28a0a2648d"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (72162-1276-3)", "package_ndc": "72162-1276-3", "marketing_start_date": "20240205"}], "brand_name": "Donepezil Hydrochloride", "product_id": "72162-1276_eac36e16-c91d-4435-97dd-089068a3efaa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "72162-1276", "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"}