Package 50228-176-30

{"route": ["ORAL"], "spl_id": "188f0dd2-baaa-4cd2-b99e-1f86225ca7b8", "openfda": {"upc": ["0350228176309", "0350228175104", "0350228175302", "0350228175050", "0350228174305", "0350228174107", "0350228174053", "0350228176101"], "unii": ["ZG7E5POY8O"], "rxcui": ["993503", "993518", "993536"], "spl_set_id": ["092da413-ec60-4577-ac57-51e3e42d55c9"], "manufacturer_name": ["ScieGen Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-01)", "package_ndc": "50228-176-01", "marketing_start_date": "20180420"}, {"sample": false, "description": "1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-10)", "package_ndc": "50228-176-10", "marketing_start_date": "20180420"}, {"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-30)", "package_ndc": "50228-176-30", "marketing_start_date": "20180420"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-60)", "package_ndc": "50228-176-60", "marketing_start_date": "20180420"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "50228-176_188f0dd2-baaa-4cd2-b99e-1f86225ca7b8", "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": "50228-176", "generic_name": "bupropion hydrochloride", "labeler_name": "ScieGen Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20180420", "listing_expiration_date": "20271231"}