Package 0228-2820-11

Brand: hydrochlorothiazide

Generic: hydrochlorothiazide
NDC Package

Package Facts

Identity

Package NDC 0228-2820-11
Digits Only 0228282011
Product NDC 0228-2820
Product ID 0228-2820_2b5bc2c3-8d3c-43c8-8e4c-e44aca5624cd
Description

100 TABLET in 1 BOTTLE (0228-2820-11)

Marketing

Marketing Status
Discontinued 2027-06-30
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": "2b5bc2c3-8d3c-43c8-8e4c-e44aca5624cd", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0302282820117"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["afdf1170-25a0-496d-b293-36ee0db2cd1e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (0228-2820-11)", "package_ndc": "0228-2820-11", "marketing_end_date": "20270630", "marketing_start_date": "20070312"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (0228-2820-96)", "package_ndc": "0228-2820-96", "marketing_end_date": "20270630", "marketing_start_date": "20231201"}], "brand_name": "Hydrochlorothiazide", "product_id": "0228-2820_2b5bc2c3-8d3c-43c8-8e4c-e44aca5624cd", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "0228-2820", "generic_name": "Hydrochlorothiazide", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040707", "marketing_category": "ANDA", "marketing_end_date": "20270630", "marketing_start_date": "20070312"}