Package 70771-1163-9

{"route": ["ORAL"], "spl_id": "2be8d068-1830-4767-9e97-8d774d9a6001", "openfda": {"unii": ["1GEV3BAW9J"], "rxcui": ["896758", "896762", "896766"], "spl_set_id": ["a3c0cc1e-1c01-4009-afdc-d35a66546aec"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70771-1163-1)", "package_ndc": "70771-1163-1", "marketing_start_date": "20171205"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70771-1163-3)", "package_ndc": "70771-1163-3", "marketing_start_date": "20171205"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70771-1163-5)", "package_ndc": "70771-1163-5", "marketing_start_date": "20171205"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70771-1163-9)", "package_ndc": "70771-1163-9", "marketing_start_date": "20171205"}], "brand_name": "Labetalol Hydrochloride", "product_id": "70771-1163_2be8d068-1830-4767-9e97-8d774d9a6001", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "70771-1163", "generic_name": "Labetalol Hydrochloride", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Labetalol Hydrochloride", "active_ingredients": [{"name": "LABETALOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA207743", "marketing_category": "ANDA", "marketing_start_date": "20171205", "listing_expiration_date": "20261231"}