hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: preferred pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler preferred pharmaceuticals inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 50 mg/1

Manufacturer
Preferred Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68788-7790
Product ID 68788-7790_4fc36bb6-717a-45a5-8964-70b4c8557242
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085182
Listing Expiration 2026-12-31
Marketing Start 2020-10-21

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 687887790
Hyphenated Format 68788-7790

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 ANDA085182 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68788-7790-0)
  • 15 TABLET in 1 BOTTLE (68788-7790-1)
  • 30 TABLET in 1 BOTTLE (68788-7790-3)
  • 60 TABLET in 1 BOTTLE (68788-7790-6)
  • 90 TABLET in 1 BOTTLE (68788-7790-9)
source: ndc

Packages (5)

68788-7790-0 100 TABLET in 1 BOTTLE (68788-7790-0) 68788-7790-1 15 TABLET in 1 BOTTLE (68788-7790-1) 68788-7790-3 30 TABLET in 1 BOTTLE (68788-7790-3) 68788-7790-6 60 TABLET in 1 BOTTLE (68788-7790-6) 68788-7790-9 90 TABLET in 1 BOTTLE (68788-7790-9)

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": "4fc36bb6-717a-45a5-8964-70b4c8557242", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["5ab641d8-cd22-4368-8070-18487dd801eb"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-7790-0)", "package_ndc": "68788-7790-0", "marketing_start_date": "20201021"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-7790-1)", "package_ndc": "68788-7790-1", "marketing_start_date": "20201021"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7790-3)", "package_ndc": "68788-7790-3", "marketing_start_date": "20201021"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7790-6)", "package_ndc": "68788-7790-6", "marketing_start_date": "20201021"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7790-9)", "package_ndc": "68788-7790-9", "marketing_start_date": "20201021"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "68788-7790_4fc36bb6-717a-45a5-8964-70b4c8557242", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68788-7790", "generic_name": "hydrochlorothiazide", "labeler_name": "Preferred 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": "20201021", "listing_expiration_date": "20261231"}