Package 50090-7511-0

{"route": ["ORAL"], "spl_id": "50dbf53d-e998-4b27-98de-df9c41df3687", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["d86e26e0-6e10-4d59-8cc8-94b551774b86"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7511-0)", "package_ndc": "50090-7511-0", "marketing_start_date": "20250220"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7511-3)", "package_ndc": "50090-7511-3", "marketing_start_date": "20250220"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "50090-7511_50dbf53d-e998-4b27-98de-df9c41df3687", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "50090-7511", "generic_name": "BUPROPION HYDROCHLORIDE", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA075491", "marketing_category": "ANDA", "marketing_start_date": "20240425", "listing_expiration_date": "20271231"}