Package 51655-390-25

{"route": ["ORAL"], "spl_id": "49dba4c8-2aab-fab0-e063-6294a90aca6d", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993687"], "spl_set_id": ["d9bbacb3-63b4-2922-e053-2a95a90a6085"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25)", "package_ndc": "51655-390-25", "marketing_start_date": "20220128"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-390-26)", "package_ndc": "51655-390-26", "marketing_start_date": "20220128"}], "brand_name": "bupropion Hydrochloride", "product_id": "51655-390_49dba4c8-2aab-fab0-e063-6294a90aca6d", "dosage_form": "TABLET", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "51655-390", "generic_name": "bupropion Hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA206975", "marketing_category": "ANDA", "marketing_start_date": "20220128", "listing_expiration_date": "20271231"}