Package 43547-290-10

{"route": ["ORAL"], "spl_id": "e8f3396b-251b-4218-9dd8-4ad0a0f8f2a2", "openfda": {"upc": ["0343547290061"], "unii": ["ZG7E5POY8O"], "rxcui": ["993503", "993518", "993536"], "spl_set_id": ["39b2d509-1281-4464-9cf1-a94bbc18b84b"], "manufacturer_name": ["Solco Healthcare US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-06)", "package_ndc": "43547-290-06", "marketing_start_date": "20141101"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-09)", "package_ndc": "43547-290-09", "marketing_start_date": "20141101"}, {"sample": false, "description": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-10)", "package_ndc": "43547-290-10", "marketing_start_date": "20141101"}, {"sample": false, "description": "500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43547-290-50)", "package_ndc": "43547-290-50", "marketing_start_date": "20141101"}], "brand_name": "bupropion hydrochloride SR", "product_id": "43547-290_e8f3396b-251b-4218-9dd8-4ad0a0f8f2a2", "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": "43547-290", "generic_name": "bupropion hydrochloride", "labeler_name": "Solco Healthcare US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bupropion hydrochloride", "brand_name_suffix": "SR", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA202304", "marketing_category": "ANDA", "marketing_start_date": "20141101", "listing_expiration_date": "20261231"}