Package 72789-158-60

{"route": ["ORAL"], "spl_id": "4af789d1-0fb9-b237-e063-6294a90a6e52", "openfda": {"upc": ["0372789158600"], "unii": ["ZG7E5POY8O"], "rxcui": ["993503"], "spl_set_id": ["9d0608a1-0cc8-491a-ad91-238e0ea009fe"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-158-60)", "package_ndc": "72789-158-60", "marketing_start_date": "20210118"}], "brand_name": "Bupropion Hydrochloride SR", "product_id": "72789-158_4af789d1-0fb9-b237-e063-6294a90a6e52", "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": "72789-158", "generic_name": "bupropion hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA205794", "marketing_category": "ANDA", "marketing_start_date": "20180420", "listing_expiration_date": "20271231"}