Package 23155-192-01

{"route": ["ORAL"], "spl_id": "b72f6124-e8e4-42b7-8095-771ff429e936", "openfda": {"upc": ["0323155191011", "0323155192018"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["9196568e-aec8-4d56-993e-4cbb78d4a3a6"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-192-01)", "package_ndc": "23155-192-01", "marketing_start_date": "20160819"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-192-10)", "package_ndc": "23155-192-10", "marketing_start_date": "20160819"}], "brand_name": "bupropion Hydrochloride", "product_id": "23155-192_b72f6124-e8e4-42b7-8095-771ff429e936", "dosage_form": "TABLET", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "23155-192", "generic_name": "bupropion Hydrochloride", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20160819", "listing_expiration_date": "20261231"}