Package 66993-188-02

{"route": ["ORAL"], "spl_id": "eca75090-9808-4673-bd7e-1ecd571d3b3e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000175557", "N0000011310"], "upc": ["0366993188027"], "unii": ["0J48LPH2TH", "27O7W4T232"], "rxcui": ["198224"], "spl_set_id": ["9d350fa2-d568-4970-a7a5-d128ff5d0a2f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Prasco Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (66993-188-02)", "package_ndc": "66993-188-02", "marketing_start_date": "20211129"}], "brand_name": "Spironolactone and Hydrochlorothiazide", "product_id": "66993-188_eca75090-9808-4673-bd7e-1ecd571d3b3e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "66993-188", "generic_name": "spironolactone and hydrochlorothiazide", "labeler_name": "Prasco Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "NDA012616", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20211129", "listing_expiration_date": "20271231"}