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 CAPSULE
Routes
ORAL
Active Ingredients

hydrochlorothiazide 12.5 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-176
Product ID 72789-176_2acfb36a-5586-8720-e063-6394a90a9a55
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203561
Listing Expiration 2026-12-31
Marketing Start 2019-01-14

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 72789176
Hyphenated Format 72789-176

Supplemental Identifiers

RxCUI
199903
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 ANDA203561 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 12.5 mg/1
source: ndc
Packaging
  • 6 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-06)
  • 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-30)
  • 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-90)
source: ndc

Packages (3)

72789-176-06 6 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-06) 72789-176-30 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-30) 72789-176-90 90 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-90)

Ingredients (1)

hydrochlorothiazide (12.5 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": "2acfb36a-5586-8720-e063-6394a90a9a55", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["199903"], "spl_set_id": ["cb7b7315-0170-492c-803f-60a6e75e55da"], "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": "6 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-06)", "package_ndc": "72789-176-06", "marketing_start_date": "20241114"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-30)", "package_ndc": "72789-176-30", "marketing_start_date": "20210318"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE, PLASTIC (72789-176-90)", "package_ndc": "72789-176-90", "marketing_start_date": "20210324"}], "brand_name": "Hydrochlorothiazide", "product_id": "72789-176_2acfb36a-5586-8720-e063-6394a90a9a55", "dosage_form": "CAPSULE", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72789-176", "generic_name": "Hydrochlorothiazide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA203561", "marketing_category": "ANDA", "marketing_start_date": "20190114", "listing_expiration_date": "20261231"}