Package 72189-349-60

{"route": ["ORAL"], "spl_id": "2c4c85cc-c2b6-ac98-e063-6294a90a973c", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993518"], "spl_set_id": ["dd4041cd-00e4-d10f-e053-2a95a90a5945"], "manufacturer_name": ["DirectRx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-30)", "package_ndc": "72189-349-30", "marketing_start_date": "20220809"}, {"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-60)", "package_ndc": "72189-349-60", "marketing_start_date": "20220422"}], "brand_name": "BUPROPION HYDROCHLORIDE SR", "product_id": "72189-349_2c4c85cc-c2b6-ac98-e063-6294a90a973c", "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": "72189-349", "generic_name": "BUPROPION HYDROCHLORIDE SR", "labeler_name": "DirectRx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPROPION HYDROCHLORIDE SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "150 mg/1"}], "application_number": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20220422", "listing_expiration_date": "20261231"}