Package 63187-713-30

{"route": ["ORAL"], "spl_id": "b5525d33-534c-440c-8a04-df329fc85056", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993541"], "spl_set_id": ["e57451fd-aba5-47d6-9892-ffe2a6021b6f"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-30)", "package_ndc": "63187-713-30", "marketing_start_date": "20160601"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-60)", "package_ndc": "63187-713-60", "marketing_start_date": "20160601"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-90)", "package_ndc": "63187-713-90", "marketing_start_date": "20160601"}], "brand_name": "Bupropion Hydrochloride", "product_id": "63187-713_b5525d33-534c-440c-8a04-df329fc85056", "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": "63187-713", "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": "ANDA077415", "marketing_category": "ANDA", "marketing_start_date": "20090501", "listing_expiration_date": "20261231"}