Package 71335-9690-3

{"route": ["ORAL"], "spl_id": "b5b49b68-10f1-4022-8ed9-d0d9294628f3", "openfda": {"nui": ["N0000000161", "N0000175556"], "unii": ["R5H8897N95"], "rxcui": ["896766"], "spl_set_id": ["0db22a64-1863-4188-850b-273ea746e327"], "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": "30 TABLET, FILM COATED in 1 BOTTLE (71335-9690-1)", "package_ndc": "71335-9690-1", "marketing_start_date": "20240403"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-9690-2)", "package_ndc": "71335-9690-2", "marketing_start_date": "20230321"}, {"sample": false, "description": "58 TABLET, FILM COATED in 1 BOTTLE (71335-9690-3)", "package_ndc": "71335-9690-3", "marketing_start_date": "20240403"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-9690-4)", "package_ndc": "71335-9690-4", "marketing_start_date": "20240403"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (71335-9690-5)", "package_ndc": "71335-9690-5", "marketing_start_date": "20240403"}], "brand_name": "Labetalol Hydrochloride", "product_id": "71335-9690_b5b49b68-10f1-4022-8ed9-d0d9294628f3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-9690", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL", "strength": "300 mg/1"}], "application_number": "ANDA075215", "marketing_category": "ANDA", "marketing_start_date": "20191122", "listing_expiration_date": "20271231"}