Package 63187-052-78

{"route": ["ORAL"], "spl_id": "73572f20-b22c-4c8c-b99e-5eb8e70f9be0", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993503", "993518", "993536"], "spl_set_id": ["d4272e3f-78ee-4d80-b911-e840fb14acbe"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-30)", "package_ndc": "63187-052-30", "marketing_start_date": "20140501"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-60)", "package_ndc": "63187-052-60", "marketing_start_date": "20140501"}, {"sample": false, "description": "180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-052-78)", "package_ndc": "63187-052-78", "marketing_start_date": "20140501"}], "brand_name": "Bupropion hydrochloride", "product_id": "63187-052_73572f20-b22c-4c8c-b99e-5eb8e70f9be0", "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": "63187-052", "generic_name": "Bupropion hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA078866", "marketing_category": "ANDA", "marketing_start_date": "20100408", "listing_expiration_date": "20261231"}