hydrochlorothiazide

Generic: hydrochlorothiazide

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

Drug Facts

Product Profile

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

hydrochlorothiazide 25 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4359
Product ID 70518-4359_3ac07946-a8b5-4392-e063-6394a90a1f75
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA085182
Listing Expiration 2026-12-31
Marketing Start 2025-06-16

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 705184359
Hyphenated Format 70518-4359

Supplemental Identifiers

RxCUI
310798
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
  • 25 mg/1
source: ndc
Packaging
  • 15 TABLET in 1 BOTTLE, PLASTIC (70518-4359-0)
  • 30 TABLET in 1 BLISTER PACK (70518-4359-1)
  • 90 TABLET in 1 BOTTLE, PLASTIC (70518-4359-2)
source: ndc

Packages (3)

70518-4359-0 15 TABLET in 1 BOTTLE, PLASTIC (70518-4359-0) 70518-4359-1 30 TABLET in 1 BLISTER PACK (70518-4359-1) 70518-4359-2 90 TABLET in 1 BOTTLE, PLASTIC (70518-4359-2)

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": "3ac07946-a8b5-4392-e063-6394a90a1f75", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["31a3d1cb-0f52-4818-965d-7584374bb23e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (70518-4359-0)", "package_ndc": "70518-4359-0", "marketing_start_date": "20250616"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4359-1)", "package_ndc": "70518-4359-1", "marketing_start_date": "20250707"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4359-2)", "package_ndc": "70518-4359-2", "marketing_start_date": "20250724"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "70518-4359_3ac07946-a8b5-4392-e063-6394a90a1f75", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-4359", "generic_name": "hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20250616", "listing_expiration_date": "20261231"}