hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler heritage pharmaceuticals inc. d/b/a avet pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 23155-009
Product ID 23155-009_a1057270-4261-4cac-bc26-2dbffb13eacb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085182
Listing Expiration 2026-12-31
Marketing Start 2015-01-15

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 23155009
Hyphenated Format 23155-009

Supplemental Identifiers

RxCUI
197770 310798 429503
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 ANDA085182 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (23155-009-01)
  • 500 TABLET in 1 BOTTLE (23155-009-05)
  • 1000 TABLET in 1 BOTTLE (23155-009-10)
  • 5000 TABLET in 1 BOTTLE (23155-009-18)
source: ndc

Packages (4)

23155-009-01 100 TABLET in 1 BOTTLE (23155-009-01) 23155-009-05 500 TABLET in 1 BOTTLE (23155-009-05) 23155-009-10 1000 TABLET in 1 BOTTLE (23155-009-10) 23155-009-18 5000 TABLET in 1 BOTTLE (23155-009-18)

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": "a1057270-4261-4cac-bc26-2dbffb13eacb", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["c59c4230-7cea-4259-9f2f-6a568716fedf"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-009-01)", "package_ndc": "23155-009-01", "marketing_start_date": "20150115"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (23155-009-05)", "package_ndc": "23155-009-05", "marketing_start_date": "20150115"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-009-10)", "package_ndc": "23155-009-10", "marketing_start_date": "20150115"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (23155-009-18)", "package_ndc": "23155-009-18", "marketing_start_date": "20150201"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "23155-009_a1057270-4261-4cac-bc26-2dbffb13eacb", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "23155-009", "generic_name": "hydrochlorothiazide", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20150115", "listing_expiration_date": "20261231"}