Package 72162-1676-5

{"route": ["ORAL"], "spl_id": "6316b7b8-5af0-40ee-bba1-2fddf79760a0", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896762"], "spl_set_id": ["3909ac9e-6818-4c5d-ad0e-52865a574b45"], "pharm_class_epc": ["beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (72162-1676-1)", "package_ndc": "72162-1676-1", "marketing_start_date": "20191122"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (72162-1676-5)", "package_ndc": "72162-1676-5", "marketing_start_date": "20191122"}], "brand_name": "Labetalol Hydrochloride", "product_id": "72162-1676_6316b7b8-5af0-40ee-bba1-2fddf79760a0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "72162-1676", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL", "strength": "200 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20191122", "listing_expiration_date": "20261231"}