Package 13668-102-90

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 13668-102-90
Digits Only 1366810290
Product NDC 13668-102
Product ID 13668-102_bc153659-2091-4682-a63b-8735e1146bac
Description

90 TABLET, FILM COATED in 1 BOTTLE (13668-102-90)

Marketing

Marketing Status
Marketed Since 2011-05-31
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": "bc153659-2091-4682-a63b-8735e1146bac", "openfda": {"upc": ["0313668102307", "0313668103304"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["76bf638e-dbde-418e-8977-1caf009990bc"], "manufacturer_name": ["Torrent Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (13668-102-05)", "package_ndc": "13668-102-05", "marketing_start_date": "20110531"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (13668-102-10)", "package_ndc": "13668-102-10", "marketing_start_date": "20110531"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (13668-102-30)", "package_ndc": "13668-102-30", "marketing_start_date": "20110531"}, {"sample": false, "description": "4000 TABLET, FILM COATED in 1 BOTTLE (13668-102-40)", "package_ndc": "13668-102-40", "marketing_start_date": "20110531"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (13668-102-90)", "package_ndc": "13668-102-90", "marketing_start_date": "20110531"}], "brand_name": "Donepezil Hydrochloride", "product_id": "13668-102_bc153659-2091-4682-a63b-8735e1146bac", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "13668-102", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Torrent Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA090686", "marketing_category": "ANDA", "marketing_start_date": "20110531", "listing_expiration_date": "20271231"}