hydrochlorothiazide

Generic: hydrochlorothiazide

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydrochlorothiazide
Generic Name hydrochlorothiazide
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-512
Product ID 72789-512_44086807-4be4-f324-e063-6394a90a0c49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA083177
Listing Expiration 2026-12-31
Marketing Start 1973-01-12

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 72789512
Hyphenated Format 72789-512

Supplemental Identifiers

RxCUI
310798
UPC
0372789512303
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 ANDA083177 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-512-30)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72789-512-60)
  • 90 TABLET in 1 BOTTLE, PLASTIC (72789-512-90)
source: ndc

Packages (3)

72789-512-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-512-30) 72789-512-60 60 TABLET in 1 BOTTLE, PLASTIC (72789-512-60) 72789-512-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-512-90)

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": "44086807-4be4-f324-e063-6394a90a0c49", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0372789512303"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["c182b6a9-1a31-45ee-9cea-a557c99f5db7"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-512-30)", "package_ndc": "72789-512-30", "marketing_start_date": "20250606"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72789-512-60)", "package_ndc": "72789-512-60", "marketing_start_date": "20251029"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-512-90)", "package_ndc": "72789-512-90", "marketing_start_date": "20250606"}], "brand_name": "Hydrochlorothiazide", "product_id": "72789-512_44086807-4be4-f324-e063-6394a90a0c49", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72789-512", "generic_name": "Hydrochlorothiazide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA083177", "marketing_category": "ANDA", "marketing_start_date": "19730112", "listing_expiration_date": "20261231"}