Package 70756-292-30

{"route": ["ORAL"], "spl_id": "2ffb359c-7e4b-44ef-a0c7-451ac966f6b6", "openfda": {"upc": ["0370756291305", "0370756291909", "0370756025306", "0370756292906", "0370756293903"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["2639abce-a5ca-4b7f-99d7-026ab3233aaa"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (70756-292-30)", "package_ndc": "70756-292-30", "marketing_start_date": "20221114"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70756-292-90)", "package_ndc": "70756-292-90", "marketing_start_date": "20221114"}], "brand_name": "Nebivolol", "product_id": "70756-292_2ffb359c-7e4b-44ef-a0c7-451ac966f6b6", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70756-292", "generic_name": "Nebivolol", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA216172", "marketing_category": "ANDA", "marketing_start_date": "20221114", "listing_expiration_date": "20261231"}