triamterene and hydrochlorothiazide (71335-2631)

Drug Facts

Product Profile

Brand Name triamterene and hydrochlorothiazide

Generic Name triamterene and hydrochlorothiazide

Labeler bryant ranch prepack

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, triamterene 37.5 mg/1

Manufacturer

Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-2631

Product ID 71335-2631_c0882d4d-0b7a-429d-aa0c-e85b4c0e1874

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA216211

Listing Expiration 2026-12-31

Marketing Start 2022-02-23

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 713352631

Hyphenated Format 71335-2631

Supplemental Identifiers

RxCUI

310812

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 ANDA216211 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
37.5 mg/1

source: ndc

Packaging

30 TABLET in 1 BOTTLE (71335-2631-1)
90 TABLET in 1 BOTTLE (71335-2631-2)
60 TABLET in 1 BOTTLE (71335-2631-3)

source: ndc

Packages (3)

71335-2631-1 30 TABLET in 1 BOTTLE (71335-2631-1) 71335-2631-2 90 TABLET in 1 BOTTLE (71335-2631-2) 71335-2631-3 60 TABLET in 1 BOTTLE (71335-2631-3)

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": "c0882d4d-0b7a-429d-aa0c-e85b4c0e1874", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812"], "spl_set_id": ["e7c34985-a8be-45d3-9273-2b13e2f6b7b2"], "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": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2631-1)", "package_ndc": "71335-2631-1", "marketing_start_date": "20250602"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-2631-2)", "package_ndc": "71335-2631-2", "marketing_start_date": "20250602"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-2631-3)", "package_ndc": "71335-2631-3", "marketing_start_date": "20250602"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "71335-2631_c0882d4d-0b7a-429d-aa0c-e85b4c0e1874", "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": "71335-2631", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "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": "ANDA216211", "marketing_category": "ANDA", "marketing_start_date": "20220223", "listing_expiration_date": "20261231"}