Package 29300-378-19

{"route": ["ORAL"], "spl_id": "1a80b28a-62f6-443e-8e8d-fc89b74be5ea", "openfda": {"upc": ["0329300375138", "0329300376135", "0329300377132", "0329300378139"], "unii": ["JGS34J7L9I"], "rxcui": ["387013", "751612", "751618", "827073"], "spl_set_id": ["b1762bbb-b5be-48a7-8101-bb736f28845a"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (29300-378-05)", "package_ndc": "29300-378-05", "marketing_start_date": "20220404"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (29300-378-13)", "package_ndc": "29300-378-13", "marketing_start_date": "20220404"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (29300-378-19)", "package_ndc": "29300-378-19", "marketing_start_date": "20220404"}], "brand_name": "Nebivolol Hydrochloride", "product_id": "29300-378_1a80b28a-62f6-443e-8e8d-fc89b74be5ea", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "29300-378", "generic_name": "Nebivolol Hydrochloride", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nebivolol Hydrochloride", "active_ingredients": [{"name": "NEBIVOLOL HYDROCHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA213830", "marketing_category": "ANDA", "marketing_start_date": "20220404", "listing_expiration_date": "20261231"}