Package 71205-419-30
Brand: hydrochlorothiazide
Generic: hydrochlorothiazidePackage Facts
Identity
Package NDC
71205-419-30
Digits Only
7120541930
Product NDC
71205-419
Description
30 TABLET in 1 BOTTLE (71205-419-30)
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": "57d5edff-ebf7-4a58-aa93-78213250d248", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0371205419301"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["ff448eb4-b48f-46f5-ac30-f03aad08f9f5"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE (71205-419-14)", "package_ndc": "71205-419-14", "marketing_start_date": "20240328"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-419-30)", "package_ndc": "71205-419-30", "marketing_start_date": "20200301"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-419-60)", "package_ndc": "71205-419-60", "marketing_start_date": "20200301"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-419-90)", "package_ndc": "71205-419-90", "marketing_start_date": "20200301"}], "brand_name": "Hydrochlorothiazide", "product_id": "71205-419_57d5edff-ebf7-4a58-aa93-78213250d248", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71205-419", "generic_name": "Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20080815", "listing_expiration_date": "20261231"}