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 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 43063-747
Product ID 43063-747_414b54cb-713c-7216-e063-6394a90af954
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202556
Listing Expiration 2026-12-31
Marketing Start 2013-04-10

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 43063747
Hyphenated Format 43063-747

Supplemental Identifiers

RxCUI
197770
UPC
0343063747018
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 ANDA202556 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (43063-747-01)
source: ndc

Packages (1)

43063-747-01 100 TABLET in 1 BOTTLE, PLASTIC (43063-747-01)

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": "414b54cb-713c-7216-e063-6394a90af954", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0343063747018"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["27a7e751-8aca-440e-95e4-cfecae1a2465"], "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": "100 TABLET in 1 BOTTLE, PLASTIC (43063-747-01)", "package_ndc": "43063-747-01", "marketing_start_date": "20170221"}], "brand_name": "Hydrochlorothiazide", "product_id": "43063-747_414b54cb-713c-7216-e063-6394a90af954", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "43063-747", "generic_name": "Hydrochlorothiazide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA202556", "marketing_category": "ANDA", "marketing_start_date": "20130410", "listing_expiration_date": "20261231"}