Package 68071-2577-3

{"route": ["ORAL"], "spl_id": "2c68b008-4863-51a9-e063-6294a90acc8b", "openfda": {"upc": ["0368071257731"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["d1043c87-0abe-ee8e-e053-2a95a90a419a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-2577-3)", "package_ndc": "68071-2577-3", "marketing_start_date": "20211117"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (68071-2577-9)", "package_ndc": "68071-2577-9", "marketing_start_date": "20250123"}], "brand_name": "Bupropion Hydrochloride", "product_id": "68071-2577_2c68b008-4863-51a9-e063-6294a90acc8b", "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": "68071-2577", "generic_name": "Bupropion Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA076143", "marketing_category": "ANDA", "marketing_start_date": "20060117", "listing_expiration_date": "20261231"}