triamterene and hydrochlorothiazide

Generic: triamterene and hydrochlorothiazide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name triamterene and hydrochlorothiazide
Generic Name triamterene and hydrochlorothiazide
Labeler bryant ranch prepack
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1, triamterene 37.5 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0504
Product ID 71335-0504_30ae3951-4e7b-4509-a2bd-fe2cd51d446c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA201407
Listing Expiration 2026-12-31
Marketing Start 2011-12-09

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 713350504
Hyphenated Format 71335-0504

Supplemental Identifiers

RxCUI
198316
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 ANDA201407 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
  • 37.5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (71335-0504-1)
  • 30 CAPSULE in 1 BOTTLE (71335-0504-2)
  • 60 CAPSULE in 1 BOTTLE (71335-0504-3)
  • 90 CAPSULE in 1 BOTTLE (71335-0504-4)
source: ndc

Packages (4)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "30ae3951-4e7b-4509-a2bd-fe2cd51d446c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["198316"], "spl_set_id": ["6517777a-e49e-4da6-b34b-66ec58cceff7"], "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": "100 CAPSULE in 1 BOTTLE (71335-0504-1)", "package_ndc": "71335-0504-1", "marketing_start_date": "20211227"}, {"sample": false, "description": "30 CAPSULE in 1 BOTTLE (71335-0504-2)", "package_ndc": "71335-0504-2", "marketing_start_date": "20200805"}, {"sample": false, "description": "60 CAPSULE in 1 BOTTLE (71335-0504-3)", "package_ndc": "71335-0504-3", "marketing_start_date": "20190423"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (71335-0504-4)", "package_ndc": "71335-0504-4", "marketing_start_date": "20200805"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "71335-0504_30ae3951-4e7b-4509-a2bd-fe2cd51d446c", "dosage_form": "CAPSULE", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71335-0504", "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": "ANDA201407", "marketing_category": "ANDA", "marketing_start_date": "20111209", "listing_expiration_date": "20261231"}