Package 65862-133-99

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 65862-133-99
Digits Only 6586213399
Product NDC 65862-133
Product ID 65862-133_db5cdbe8-1cd9-4bc3-a9b3-4fb4f053db3e
Description

1000 TABLET in 1 BOTTLE (65862-133-99)

Marketing

Marketing Status
Marketed Since 2007-07-20
Brand hydrochlorothiazide
Generic hydrochlorothiazide
Sample Package No

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "db5cdbe8-1cd9-4bc3-a9b3-4fb4f053db3e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798"], "spl_set_id": ["01f1f478-5493-439f-9b99-f4f82023781c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (65862-133-01)", "package_ndc": "65862-133-01", "marketing_start_date": "20070720"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (65862-133-99)", "package_ndc": "65862-133-99", "marketing_start_date": "20070720"}], "brand_name": "Hydrochlorothiazide", "product_id": "65862-133_db5cdbe8-1cd9-4bc3-a9b3-4fb4f053db3e", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "65862-133", "generic_name": "Hydrochlorothiazide", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040780", "marketing_category": "ANDA", "marketing_start_date": "20070720", "listing_expiration_date": "20261231"}