Package 43547-460-09

{"route": ["ORAL"], "spl_id": "745438ab-c3fe-4da9-9548-730970399e0d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "R85M2X0D68"], "rxcui": ["578325", "578330", "802749"], "spl_set_id": ["543b9806-ccfa-4144-a2a2-d0e35eaceeee"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Solco Healthcare LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (43547-460-09)", "package_ndc": "43547-460-09", "marketing_start_date": "20171120"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (43547-460-50)", "package_ndc": "43547-460-50", "marketing_start_date": "20171120"}], "brand_name": "candesartan cilexetil and hydrochlorothiazide", "product_id": "43547-460_745438ab-c3fe-4da9-9548-730970399e0d", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "43547-460", "generic_name": "candesartan cilexetil and hydrochlorothiazide", "labeler_name": "Solco Healthcare LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "candesartan cilexetil and hydrochlorothiazide", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "32 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA207455", "marketing_category": "ANDA", "marketing_start_date": "20171120", "listing_expiration_date": "20261231"}