Package 43547-276-03

{"route": ["ORAL"], "spl_id": "dcfd9a94-e1bc-4b53-ae6f-0200ee714917", "openfda": {"upc": ["0343547276034", "0343547275037"], "unii": ["3O2T2PJ89D"], "rxcui": ["997223", "997229"], "spl_set_id": ["042a59ea-131a-4806-b0f4-2f791d4414e2"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-03)", "package_ndc": "43547-276-03", "marketing_start_date": "20111101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-09)", "package_ndc": "43547-276-09", "marketing_start_date": "20111101"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43547-276-11)", "package_ndc": "43547-276-11", "marketing_start_date": "20111101"}], "brand_name": "donepezil hydrochloride", "product_id": "43547-276_dcfd9a94-e1bc-4b53-ae6f-0200ee714917", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "43547-276", "generic_name": "donepezil hydrochloride", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "donepezil hydrochloride", "active_ingredients": [{"name": "DONEPEZIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA200292", "marketing_category": "ANDA", "marketing_start_date": "20111101", "listing_expiration_date": "20261231"}