triamterene and hydrochlorothiazide (72789-183)

Drug Facts

Product Profile

Brand Name triamterene and hydrochlorothiazide

Generic Name triamterene and hydrochlorothiazide

Labeler pd-rx pharmaceuticals, inc.

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, triamterene 37.5 mg/1

Manufacturer

PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-183

Product ID 72789-183_4b070993-0f47-b372-e063-6394a90a98ad

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA071251

Listing Expiration 2027-12-31

Marketing Start 2009-09-21

Pharmacologic Class

Established (EPC)

thiazide diuretic [epc] potassium-sparing diuretic [epc]

Chemical Structure

thiazides [cs]

Physiologic Effect

increased diuresis [pe] decreased renal k+ excretion [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789183

Hyphenated Format 72789-183

Supplemental Identifiers

RxCUI

310812

UPC

0372789183909

UNII

0J48LPH2TH WS821Z52LQ

NUI

N0000175359 N0000175419 M0471776 N0000008859 N0000175418

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 triamterene and hydrochlorothiazide (source: ndc)

Generic Name triamterene and hydrochlorothiazide (source: ndc)

Application Number ANDA071251 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
37.5 mg/1

source: ndc

Packaging

30 TABLET in 1 BOTTLE, PLASTIC (72789-183-30)
90 TABLET in 1 BOTTLE, PLASTIC (72789-183-90)

source: ndc

Packages (2)

72789-183-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-183-30) 72789-183-90 90 TABLET in 1 BOTTLE, PLASTIC (72789-183-90)

Ingredients (2)

hydrochlorothiazide (25 mg/1) triamterene (37.5 mg/1)

Linked Drug Pages (1)

Triamterene and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "4b070993-0f47-b372-e063-6394a90a98ad", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "upc": ["0372789183909"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812"], "spl_set_id": ["f083c321-3170-4982-b5cd-d3fdff754857"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]", "Decreased Renal K+ Excretion [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Potassium-sparing Diuretic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-183-30)", "package_ndc": "72789-183-30", "marketing_start_date": "20210604"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-183-90)", "package_ndc": "72789-183-90", "marketing_start_date": "20210531"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "72789-183_4b070993-0f47-b372-e063-6394a90a98ad", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72789-183", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamterene and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "TRIAMTERENE", "strength": "37.5 mg/1"}], "application_number": "ANDA071251", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20271231"}