hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: unichem pharmaceuticals (usa), inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler unichem pharmaceuticals (usa), inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1

Manufacturer
Unichem Pharmaceuticals (USA), Inc.

Identifiers & Regulatory

Product NDC 29300-128
Product ID 29300-128_1e92de42-a7f2-4674-8260-28cfabf0759d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040907
Listing Expiration 2026-12-31
Marketing Start 2008-08-15

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 29300128
Hyphenated Format 29300-128

Supplemental Identifiers

RxCUI
197770 310798 429503
UPC
0329300129014 0329300128017
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 ANDA040907 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (29300-128-01)
  • 500 TABLET in 1 BOTTLE (29300-128-05)
  • 1000 TABLET in 1 BOTTLE (29300-128-10)
  • 5000 TABLET in 1 BOTTLE (29300-128-50)
source: ndc

Packages (4)

29300-128-01 100 TABLET in 1 BOTTLE (29300-128-01) 29300-128-05 500 TABLET in 1 BOTTLE (29300-128-05) 29300-128-10 1000 TABLET in 1 BOTTLE (29300-128-10) 29300-128-50 5000 TABLET in 1 BOTTLE (29300-128-50)

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": "1e92de42-a7f2-4674-8260-28cfabf0759d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0329300129014", "0329300128017"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["33f3b980-b339-4dbf-99bd-05588c2a298c"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Unichem Pharmaceuticals (USA), Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (29300-128-01)", "package_ndc": "29300-128-01", "marketing_start_date": "20090702"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (29300-128-05)", "package_ndc": "29300-128-05", "marketing_start_date": "20090702"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (29300-128-10)", "package_ndc": "29300-128-10", "marketing_start_date": "20090702"}, {"sample": false, "description": "5000 TABLET in 1 BOTTLE (29300-128-50)", "package_ndc": "29300-128-50", "marketing_start_date": "20090702"}], "brand_name": "Hydrochlorothiazide", "product_id": "29300-128_1e92de42-a7f2-4674-8260-28cfabf0759d", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "29300-128", "generic_name": "Hydrochlorothiazide", "labeler_name": "Unichem Pharmaceuticals (USA), Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20080815", "listing_expiration_date": "20261231"}