Package 67046-1476-3

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1476-3
Digits Only 6704614763
Product NDC 67046-1476
Product ID 67046-1476_2d01f6be-2eb0-8f47-e063-6394a90a56af
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1476-3)

Marketing

Marketing Status
Marketed Since 2025-01-31
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": "2d01f6be-2eb0-8f47-e063-6394a90a56af", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997229"], "spl_set_id": ["2d01fb96-c825-fad5-e063-6394a90ac6cc"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1476-3)", "package_ndc": "67046-1476-3", "marketing_start_date": "20250131"}], "brand_name": "Donepezil Hydrochloride", "product_id": "67046-1476_2d01f6be-2eb0-8f47-e063-6394a90a56af", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "67046-1476", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Coupler LLC", "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": "20250131", "listing_expiration_date": "20261231"}