Package 70518-4380-0

Brand: donepezil

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4380-0
Digits Only 7051843800
Product NDC 70518-4380
Product ID 70518-4380_38f267b8-b95d-f393-e063-6294a90ad5be
Description

90 TABLET in 1 BOTTLE, PLASTIC (70518-4380-0)

Marketing

Marketing Status
Marketed Since 2025-07-01
Brand donepezil
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (1)

Donepezil ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "38f267b8-b95d-f393-e063-6294a90ad5be", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["37fc6638-4a63-4582-a64c-3525f8ed7ef2"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4380-0)", "package_ndc": "70518-4380-0", "marketing_start_date": "20250701"}], "brand_name": "Donepezil", "product_id": "70518-4380_38f267b8-b95d-f393-e063-6294a90ad5be", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "70518-4380", "generic_name": "Donepezil hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA203034", "marketing_category": "ANDA", "marketing_start_date": "20250701", "listing_expiration_date": "20261231"}