Package 33342-028-12

Brand: donepezil hydrochloride

Generic: donepezil hydrochloride
NDC Package

Package Facts

Identity

Package NDC 33342-028-12
Digits Only 3334202812
Product NDC 33342-028
Description

10 BLISTER PACK in 1 CARTON (33342-028-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2012-08-17
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": "4bf742a3-3c8f-4bd3-b973-54370cbef345", "openfda": {"upc": ["0333342061102", "0333342061072", "0333342030078", "0333342027108", "0333342027078", "0333342029072", "0333342029607", "0333342027153", "0333342028150", "0333342030603"], "unii": ["3O2T2PJ89D"], "rxcui": ["997220", "997223", "997226", "997229", "1100184"], "spl_set_id": ["06dd25a5-1bf2-446d-ad75-ff9d55117660"], "manufacturer_name": ["Macleods Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (33342-028-07)", "package_ndc": "33342-028-07", "marketing_start_date": "20120817"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (33342-028-10)", "package_ndc": "33342-028-10", "marketing_start_date": "20120817"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (33342-028-12)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-028-12", "marketing_start_date": "20120817"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (33342-028-15)", "package_ndc": "33342-028-15", "marketing_start_date": "20141106"}, {"sample": false, "description": "5 BLISTER PACK in 1 CARTON (33342-028-31)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "33342-028-31", "marketing_start_date": "20120817"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (33342-028-44)", "package_ndc": "33342-028-44", "marketing_start_date": "20141106"}], "brand_name": "Donepezil Hydrochloride", "product_id": "33342-028_4bf742a3-3c8f-4bd3-b973-54370cbef345", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "33342-028", "generic_name": "Donepezil Hydrochloride", "labeler_name": "Macleods Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Donepezil Hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA201146", "marketing_category": "ANDA", "marketing_start_date": "20120817", "listing_expiration_date": "20261231"}