Package 0904-6478-61

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0904-6478-61
Digits Only 0904647861
Product NDC 0904-6478
Product ID 0904-6478_cb092ac4-5569-4fbf-88bd-8b3037a946fb
Description

100 BLISTER PACK in 1 CARTON (0904-6478-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2011-05-28
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": "cb092ac4-5569-4fbf-88bd-8b3037a946fb", "openfda": {"unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["c777ddc9-0b61-4d6f-95d6-818ba1861d62"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-6478-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-6478-61", "marketing_start_date": "20110528"}], "brand_name": "Donepezil Hydrochloride", "product_id": "0904-6478_cb092ac4-5569-4fbf-88bd-8b3037a946fb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "0904-6478", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA090686", "marketing_category": "ANDA", "marketing_start_date": "20110528", "listing_expiration_date": "20271231"}