Package 24979-004-07

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 24979-004-07
Digits Only 2497900407
Product NDC 24979-004
Product ID 24979-004_e1f7708c-55a7-4201-86c6-089ff0cce422
Description

90 TABLET, FILM COATED in 1 BOTTLE (24979-004-07)

Marketing

Marketing Status
Marketed Since 2015-09-22
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": "e1f7708c-55a7-4201-86c6-089ff0cce422", "openfda": {"upc": ["0324979004068", "0324979004075"], "unii": ["3O2T2PJ89D"], "rxcui": ["1100184"], "spl_set_id": ["12a755c5-1ad9-43d1-832a-eb2ff17bd693"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (24979-004-06)", "package_ndc": "24979-004-06", "marketing_start_date": "20150301"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (24979-004-07)", "package_ndc": "24979-004-07", "marketing_start_date": "20150922"}], "brand_name": "Donepezil Hydrochloride", "product_id": "24979-004_e1f7708c-55a7-4201-86c6-089ff0cce422", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "24979-004", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "23 mg/1"}], "application_number": "ANDA203104", "marketing_category": "ANDA", "marketing_start_date": "20150301", "listing_expiration_date": "20261231"}