Package 50090-1150-0

{"route": ["ORAL"], "spl_id": "f3c02405-f0db-47fe-b943-fa20fdc1f432", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["1801289"], "spl_set_id": ["dfb45438-1116-48f2-9bfe-776ebbf1e119"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50090-1150-0)", "package_ndc": "50090-1150-0", "marketing_start_date": "20141128"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-1150-1)", "package_ndc": "50090-1150-1", "marketing_start_date": "20141128"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "50090-1150_f3c02405-f0db-47fe-b943-fa20fdc1f432", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-1150", "generic_name": "bupropion hydrochloride", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA079094", "marketing_category": "ANDA", "marketing_start_date": "20090611", "listing_expiration_date": "20261231"}