Package 82009-119-05

Brand: donepezil

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 82009-119-05
Digits Only 8200911905
Product NDC 82009-119
Product ID 82009-119_4533e92e-9af5-cce3-e063-6294a90ac926
Description

500 TABLET in 1 BOTTLE (82009-119-05)

Marketing

Marketing Status
Marketed Since 2023-07-19
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": "4533e92e-9af5-cce3-e063-6294a90ac926", "openfda": {"upc": ["0382009119052", "0382009120058"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["c7e1f642-1bdc-4ed6-9b9e-c1af40b926cd"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (82009-119-05)", "package_ndc": "82009-119-05", "marketing_start_date": "20230719"}], "brand_name": "Donepezil", "product_id": "82009-119_4533e92e-9af5-cce3-e063-6294a90ac926", "dosage_form": "TABLET", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "82009-119", "generic_name": "Donepezil hydrochloride", "labeler_name": "Quallent Pharmaceuticals Health LLC", "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": "20230719", "listing_expiration_date": "20261231"}