Package 46708-118-91

{"route": ["ORAL"], "spl_id": "b09bdaa7-0871-4741-b5cd-dd30d683613c", "openfda": {"upc": ["0346708127312", "0346708118310"], "unii": ["ZG7E5POY8O"], "rxcui": ["993687", "993691"], "spl_set_id": ["ef0bb8f2-7710-4236-8b47-57b74c8bca3e"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-118-31)", "package_ndc": "46708-118-31", "marketing_start_date": "20180618"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (46708-118-91)", "package_ndc": "46708-118-91", "marketing_start_date": "20180618"}], "brand_name": "Bupropion Hydrochloride", "product_id": "46708-118_b09bdaa7-0871-4741-b5cd-dd30d683613c", "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": "46708-118", "generic_name": "Bupropion Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bupropion Hydrochloride", "active_ingredients": [{"name": "BUPROPION HYDROCHLORIDE", "strength": "75 mg/1"}], "application_number": "ANDA203013", "marketing_category": "ANDA", "marketing_start_date": "20180618", "listing_expiration_date": "20261231"}