Package 60505-0158-1

{"route": ["ORAL"], "spl_id": "cf3f7cdc-3541-a71a-08c5-a74345180a3e", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["86530199-999b-9f92-b1bc-b8515ec829f3"], "manufacturer_name": ["Apotex Corp"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60505-0158-1)", "package_ndc": "60505-0158-1", "marketing_start_date": "20060117"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (60505-0158-3)", "package_ndc": "60505-0158-3", "marketing_start_date": "20060117"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (60505-0158-5)", "package_ndc": "60505-0158-5", "marketing_start_date": "20060117"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (60505-0158-7)", "package_ndc": "60505-0158-7", "marketing_start_date": "20060117"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (60505-0158-9)", "package_ndc": "60505-0158-9", "marketing_start_date": "20060117"}], "brand_name": "Bupropion Hydrochloride", "product_id": "60505-0158_cf3f7cdc-3541-a71a-08c5-a74345180a3e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "60505-0158", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Apotex Corp", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}