Package 71335-2346-1

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-2346-1
Digits Only 7133523461
Product NDC 71335-2346
Description

30 TABLET, FILM COATED in 1 BOTTLE (71335-2346-1)

Marketing

Marketing Status
Marketed Since 2024-02-06
Brand donepezil hydrochloride
Generic donepezil hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d51b7603-3e3f-470a-bece-b81e13dab4fd", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223"], "spl_set_id": ["1c6e8d7f-5219-4b6c-a1ce-2baff28c3d55"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2346-1)", "package_ndc": "71335-2346-1", "marketing_start_date": "20240206"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2346-2)", "package_ndc": "71335-2346-2", "marketing_start_date": "20240206"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2346-3)", "package_ndc": "71335-2346-3", "marketing_start_date": "20240206"}], "brand_name": "Donepezil Hydrochloride", "product_id": "71335-2346_d51b7603-3e3f-470a-bece-b81e13dab4fd", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "71335-2346", "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": "10 mg/1"}], "application_number": "ANDA090056", "marketing_category": "ANDA", "marketing_start_date": "20110531", "listing_expiration_date": "20261231"}