hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 82804-972
Product ID 82804-972_4c1a2fb9-133d-4bd5-a336-e47d54f22c97
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA087059
Listing Expiration 2026-12-31
Marketing Start 2020-09-25

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 82804972
Hyphenated Format 82804-972

Supplemental Identifiers

RxCUI
197770 310798
UPC
0382804973309 0382804972302
UNII
0J48LPH2TH
NUI
N0000175359 N0000175419 M0471776

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 ANDA087059 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (82804-972-00)
  • 1000 TABLET in 1 BOTTLE (82804-972-11)
  • 30 TABLET in 1 BOTTLE (82804-972-30)
  • 500 TABLET in 1 BOTTLE (82804-972-55)
  • 60 TABLET in 1 BOTTLE (82804-972-60)
  • 120 TABLET in 1 BOTTLE (82804-972-72)
  • 90 TABLET in 1 BOTTLE (82804-972-90)
source: ndc

Packages (7)

82804-972-00 100 TABLET in 1 BOTTLE (82804-972-00) 82804-972-11 1000 TABLET in 1 BOTTLE (82804-972-11) 82804-972-30 30 TABLET in 1 BOTTLE (82804-972-30) 82804-972-55 500 TABLET in 1 BOTTLE (82804-972-55) 82804-972-60 60 TABLET in 1 BOTTLE (82804-972-60) 82804-972-72 120 TABLET in 1 BOTTLE (82804-972-72) 82804-972-90 90 TABLET in 1 BOTTLE (82804-972-90)

Ingredients (1)

hydrochlorothiazide (25 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": "4c1a2fb9-133d-4bd5-a336-e47d54f22c97", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0382804973309", "0382804972302"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798"], "spl_set_id": ["4c1a2fb9-133d-4bd5-a336-e47d54f22c97"], "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": "100 TABLET in 1 BOTTLE (82804-972-00)", "package_ndc": "82804-972-00", "marketing_start_date": "20250213"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82804-972-11)", "package_ndc": "82804-972-11", "marketing_start_date": "20250213"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-972-30)", "package_ndc": "82804-972-30", "marketing_start_date": "20250213"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82804-972-55)", "package_ndc": "82804-972-55", "marketing_start_date": "20250213"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (82804-972-60)", "package_ndc": "82804-972-60", "marketing_start_date": "20250213"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (82804-972-72)", "package_ndc": "82804-972-72", "marketing_start_date": "20250213"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-972-90)", "package_ndc": "82804-972-90", "marketing_start_date": "20250213"}], "brand_name": "Hydrochlorothiazide", "product_id": "82804-972_4c1a2fb9-133d-4bd5-a336-e47d54f22c97", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "82804-972", "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": "ANDA087059", "marketing_category": "ANDA", "marketing_start_date": "20200925", "listing_expiration_date": "20261231"}