Package 69367-219-01

{"route": ["ORAL"], "spl_id": "43b28163-bdd8-4531-9532-1624c5ef198c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["0fc94bc2-fa38-439a-a609-1b4130cdacb1"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Westminster Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-01)", "package_ndc": "69367-219-01", "marketing_start_date": "20190607"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-05)", "package_ndc": "69367-219-05", "marketing_start_date": "20190607"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE, PLASTIC (69367-219-10)", "package_ndc": "69367-219-10", "marketing_start_date": "20190607"}], "brand_name": "Hydrochlorothiazide", "product_id": "69367-219_43b28163-bdd8-4531-9532-1624c5ef198c", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "69367-219", "generic_name": "Hydrochlorothiazide", "labeler_name": "Westminster Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA203561", "marketing_category": "ANDA", "marketing_start_date": "20190607", "listing_expiration_date": "20261231"}