Package 63187-726-90

{"route": ["ORAL"], "spl_id": "d2ba7af1-c874-47ab-b638-be94dfe1b1dd", "openfda": {"upc": ["0363187726300"], "unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["13770e60-117c-4814-93bb-9bc41a042a20"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-30)", "package_ndc": "63187-726-30", "marketing_start_date": "20160701"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-60)", "package_ndc": "63187-726-60", "marketing_start_date": "20160701"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (63187-726-90)", "package_ndc": "63187-726-90", "marketing_start_date": "20160701"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "63187-726_d2ba7af1-c874-47ab-b638-be94dfe1b1dd", "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": "63187-726", "generic_name": "bupropion hydrochloride", "labeler_name": "Proficient Rx LP", "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": "ANDA079095", "marketing_category": "ANDA", "marketing_start_date": "20090702", "listing_expiration_date": "20261231"}