hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: actavis pharma, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler actavis pharma, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1

Manufacturer
Actavis Pharma, Inc.

Identifiers & Regulatory

Product NDC 0228-2820
Product ID 0228-2820_2b5bc2c3-8d3c-43c8-8e4c-e44aca5624cd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040707
Marketing Start 2007-03-12
Marketing End 2027-06-30

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 02282820
Hyphenated Format 0228-2820

Supplemental Identifiers

RxCUI
429503
UPC
0302282820117
UNII
0J48LPH2TH
NUI
N0000175359 N0000175419 M0471776

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name hydrochlorothiazide (source: ndc)
Generic Name hydrochlorothiazide (source: ndc)
Application Number ANDA040707 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (0228-2820-11)
  • 1000 TABLET in 1 BOTTLE (0228-2820-96)
source: ndc

Packages (2)

0228-2820-11 100 TABLET in 1 BOTTLE (0228-2820-11) 0228-2820-96 1000 TABLET in 1 BOTTLE (0228-2820-96)

Ingredients (1)

hydrochlorothiazide (12.5 mg/1)

Linked Drug Pages (1)

Hydrochlorothiazide ndc-match (0.9)

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"}