Package 71335-2169-1

{"route": ["ORAL"], "spl_id": "10871eff-034a-41ec-9f59-2bd2cc7891ef", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896762"], "spl_set_id": ["04f9dcdf-4023-48ee-9e7d-ca9366d9db72"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2169-1)", "package_ndc": "71335-2169-1", "marketing_start_date": "20220906"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2169-2)", "package_ndc": "71335-2169-2", "marketing_start_date": "20220906"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-2169-3)", "package_ndc": "71335-2169-3", "marketing_start_date": "20220906"}], "brand_name": "LABETALOL HYDROCHLORIDE", "product_id": "71335-2169_10871eff-034a-41ec-9f59-2bd2cc7891ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-2169", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LABETALOL HYDROCHLORIDE", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "200 mg/1"}], "application_number": "ANDA211953", "marketing_category": "ANDA", "marketing_start_date": "20210818", "listing_expiration_date": "20261231"}