Package 60760-662-90
Brand: hydrochlorothiazide
Generic: hydrochlorothiazidePackage Facts
Identity
Package NDC
60760-662-90
Digits Only
6076066290
Product NDC
60760-662
Description
90 TABLET in 1 BOTTLE, PLASTIC (60760-662-90)
Marketing
Marketing Status
Brand
hydrochlorothiazide
Generic
hydrochlorothiazide
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0994a032-bcfd-d389-e063-6294a90afbe0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["099496f1-4e2d-8d21-e063-6294a90af695"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-662-90)", "package_ndc": "60760-662-90", "marketing_start_date": "20231024"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "60760-662_0994a032-bcfd-d389-e063-6294a90afbe0", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "60760-662", "generic_name": "HYDROCHLOROTHIAZIDE", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040702", "marketing_category": "ANDA", "marketing_start_date": "20191101", "listing_expiration_date": "20261231"}