Package 72789-070-30

{"route": ["ORAL"], "spl_id": "3ca55d80-dd83-16fb-e063-6294a90afa4b", "openfda": {"upc": ["0372789070902"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["867d3876-6974-4e89-bc45-9e60e84b401c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-30)", "package_ndc": "72789-070-30", "marketing_start_date": "20200326"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-070-90)", "package_ndc": "72789-070-90", "marketing_start_date": "20240607"}], "brand_name": "Bupropion Hydrochloride", "product_id": "72789-070_3ca55d80-dd83-16fb-e063-6294a90afa4b", "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": "72789-070", "generic_name": "Bupropion Hydrochloride", "labeler_name": "PD-Rx 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"}