Package 71209-061-11

{"route": ["ORAL"], "spl_id": "0ab335f1-2089-496b-b65f-02c697f6ee89", "openfda": {"upc": ["0371209060042", "0371209060059", "0371209058056"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["451cdd6e-13b4-402f-8a44-cdf5f7433a49"], "manufacturer_name": ["Cadila Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71209-061-01)", "package_ndc": "71209-061-01", "marketing_start_date": "20181016"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71209-061-04)", "package_ndc": "71209-061-04", "marketing_start_date": "20181016"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71209-061-05)", "package_ndc": "71209-061-05", "marketing_start_date": "20181016"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71209-061-11)", "package_ndc": "71209-061-11", "marketing_start_date": "20181016"}], "brand_name": "Nebivolol", "product_id": "71209-061_0ab335f1-2089-496b-b65f-02c697f6ee89", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71209-061", "generic_name": "Nebivolol", "labeler_name": "Cadila Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA208717", "marketing_category": "ANDA", "marketing_start_date": "20171229", "listing_expiration_date": "20261231"}