Package 0172-2083-80

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 0172-2083-80
Digits Only 0172208380
Product NDC 0172-2083
Product ID 0172-2083_6659686c-94ec-408c-b0bb-c78528aaa6c0
Description

1000 TABLET in 1 BOTTLE (0172-2083-80)

Marketing

Marketing Status
Marketed Since 1973-01-12
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": "6659686c-94ec-408c-b0bb-c78528aaa6c0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0301722083600", "0301723444608"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["e2270db4-2930-4ec5-ac96-2b4542aed367"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0172-2083-60)", "package_ndc": "0172-2083-60", "marketing_start_date": "19730112"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0172-2083-80)", "package_ndc": "0172-2083-80", "marketing_start_date": "19730112"}], "brand_name": "Hydrochlorothiazide", "product_id": "0172-2083_6659686c-94ec-408c-b0bb-c78528aaa6c0", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "0172-2083", "generic_name": "Hydrochlorothiazide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA083177", "marketing_category": "ANDA", "marketing_start_date": "19730112", "listing_expiration_date": "20261231"}