Package 16714-937-01

{"route": ["ORAL"], "spl_id": "8ca5026f-56b1-4f46-96f0-a36ace459fb5", "openfda": {"nui": ["N0000175359", "N0000175420", "N0000000161", "N0000175556"], "unii": ["Q0MQD1073Q", "50VV3VW0TI"], "rxcui": ["197382", "197383"], "spl_set_id": ["1494d5f7-8620-46da-8bca-69b76cd17635"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "pharm_class_moa": ["Adrenergic beta-Antagonists [MoA]"], "manufacturer_name": ["Northstar Rx LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-937-01)", "package_ndc": "16714-937-01", "marketing_start_date": "20190326"}], "brand_name": "Atenolol and Chlorthalidone", "product_id": "16714-937_8ca5026f-56b1-4f46-96f0-a36ace459fb5", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide-like Diuretic [EPC]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "16714-937", "generic_name": "Atenolol and Chlorthalidone", "labeler_name": "Northstar Rx LLC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atenolol and Chlorthalidone", "active_ingredients": [{"name": "ATENOLOL", "strength": "100 mg/1"}, {"name": "CHLORTHALIDONE", "strength": "25 mg/1"}], "application_number": "ANDA210028", "marketing_category": "ANDA", "marketing_start_date": "20190326", "listing_expiration_date": "20261231"}