Package 70518-4392-0

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4392-0
Digits Only 7051843920
Product NDC 70518-4392
Product ID 70518-4392_3a0b2193-f0a9-26aa-e063-6294a90a8368
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4392-0)

Marketing

Marketing Status
Marketed Since 2025-07-15
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": "3a0b2193-f0a9-26aa-e063-6294a90a8368", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["de96349a-5fee-4de9-921c-e453d44b3203"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4392-0)", "package_ndc": "70518-4392-0", "marketing_start_date": "20250715"}], "brand_name": "Donepezil Hydrochloride", "product_id": "70518-4392_3a0b2193-f0a9-26aa-e063-6294a90a8368", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "70518-4392", "generic_name": "Donepezil Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090056", "marketing_category": "ANDA", "marketing_start_date": "20250715", "listing_expiration_date": "20261231"}