hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: golden state medical supply, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler golden state medical supply, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
Golden State Medical Supply, Inc.

Identifiers & Regulatory

Product NDC 51407-332
Product ID 51407-332_21e0275e-8868-abe8-e063-6294a90ae2b2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040702
Listing Expiration 2026-12-31
Marketing Start 2007-03-16

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 51407332
Hyphenated Format 51407-332

Supplemental Identifiers

RxCUI
197770 310798 429503
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 ANDA040702 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (51407-332-01)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (51407-332-10)
  • 90 TABLET in 1 BOTTLE, PLASTIC (51407-332-90)
source: ndc

Packages (3)

51407-332-01 100 TABLET in 1 BOTTLE, PLASTIC (51407-332-01) 51407-332-10 1000 TABLET in 1 BOTTLE, PLASTIC (51407-332-10) 51407-332-90 90 TABLET in 1 BOTTLE, PLASTIC (51407-332-90)

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": "21e0275e-8868-abe8-e063-6294a90ae2b2", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798", "429503"], "spl_set_id": ["a85f69f5-ba97-478d-e053-2a95a90a0a97"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Golden State Medical Supply, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (51407-332-01)", "package_ndc": "51407-332-01", "marketing_start_date": "20200617"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (51407-332-10)", "package_ndc": "51407-332-10", "marketing_start_date": "20200617"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51407-332-90)", "package_ndc": "51407-332-90", "marketing_start_date": "20200617"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "51407-332_21e0275e-8868-abe8-e063-6294a90ae2b2", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "51407-332", "generic_name": "HYDROCHLOROTHIAZIDE", "labeler_name": "Golden State Medical Supply, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA040702", "marketing_category": "ANDA", "marketing_start_date": "20070316", "listing_expiration_date": "20261231"}