Package 55700-820-90

{"route": ["ORAL"], "spl_id": "56942110-9635-4106-a616-e227284026ab", "openfda": {"unii": ["ZG7E5POY8O"], "rxcui": ["993557"], "spl_set_id": ["a225dbbb-86f0-4547-a1c8-68eb64cd6892"], "manufacturer_name": ["Quality Care Products, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-30)", "package_ndc": "55700-820-30", "marketing_end_date": "20260831", "marketing_start_date": "20191122"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (55700-820-90)", "package_ndc": "55700-820-90", "marketing_end_date": "20260331", "marketing_start_date": "20201112"}], "brand_name": "BUPROPION HYDROCHLORIDE", "product_id": "55700-820_56942110-9635-4106-a616-e227284026ab", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Aminoketone [EPC]", "Dopamine Uptake Inhibitors [MoA]", "Increased Dopamine Activity [PE]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Uptake Inhibitors [MoA]"], "product_ndc": "55700-820", "generic_name": "BUPROPION HYDROCHLORIDE", "labeler_name": "Quality Care Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BUPROPION HYDROCHLORIDE", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "300 mg/1"}], "application_number": "ANDA210497", "marketing_category": "ANDA", "marketing_end_date": "20260831", "marketing_start_date": "20191122"}