Package 69097-973-07

{"route": ["ORAL"], "spl_id": "25e66ad5-947a-4262-a996-a9695601d301", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0369097973070", "0369097972073"], "unii": ["0J48LPH2TH", "NW2RTH6T2N"], "rxcui": ["857166", "857174"], "spl_set_id": ["4e1ed7da-029e-48d6-a5e4-fc7ac11192fb"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["CIPLA USA INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69097-973-07)", "package_ndc": "69097-973-07", "marketing_start_date": "20200724"}], "brand_name": "Fosinopril Sodium and Hydrochlorothiazide", "product_id": "69097-973_25e66ad5-947a-4262-a996-a9695601d301", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "69097-973", "generic_name": "Fosinopril Sodium and Hydrochlorothiazide", "labeler_name": "CIPLA USA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fosinopril Sodium and Hydrochlorothiazide", "active_ingredients": [{"name": "FOSINOPRIL SODIUM", "strength": "20 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA090228", "marketing_category": "ANDA", "marketing_start_date": "20200724", "listing_expiration_date": "20261231"}