Package 70518-4517-0

{"route": ["ORAL"], "spl_id": "43431591-01e3-99e0-e063-6294a90a2e74", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403854"], "spl_set_id": ["206cd386-cf38-4e0f-80ec-685aea41b048"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4517-0)", "package_ndc": "70518-4517-0", "marketing_start_date": "20251110"}], "brand_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "product_id": "70518-4517_43431591-01e3-99e0-e063-6294a90a2e74", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-4517", "generic_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA204801", "marketing_category": "ANDA", "marketing_start_date": "20251110", "listing_expiration_date": "20261231"}