hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: direct rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

hydrochlorothiazide 50 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-263
Product ID 72189-263_2c29005f-2597-e87a-e063-6294a90a2fc3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202556
Listing Expiration 2026-12-31
Marketing Start 2021-09-13

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 72189263
Hyphenated Format 72189-263

Supplemental Identifiers

RxCUI
197770
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 ANDA202556 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (72189-263-90)
source: ndc

Packages (1)

72189-263-90 90 TABLET in 1 BOTTLE (72189-263-90)

Ingredients (1)

hydrochlorothiazide (50 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": "2c29005f-2597-e87a-e063-6294a90a2fc3", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["cbe5e01e-67ca-f8a2-e053-2995a90a0d15"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (72189-263-90)", "package_ndc": "72189-263-90", "marketing_start_date": "20210913"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "72189-263_2c29005f-2597-e87a-e063-6294a90a2fc3", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72189-263", "generic_name": "HYDROCHLOROTHIAZIDE", "labeler_name": "DIRECT RX", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA202556", "marketing_category": "ANDA", "marketing_start_date": "20210913", "listing_expiration_date": "20261231"}