triamterene and hydrochlorothiazide (0781-2074)

Drug Facts

Product Profile

Brand Name triamterene and hydrochlorothiazide

Generic Name triamterene and hydrochlorothiazide

Labeler sandoz inc

Dosage Form CAPSULE

Routes

ORAL

Active Ingredients

hydrochlorothiazide 25 mg/1, triamterene 37.5 mg/1

Manufacturer

Sandoz Inc

Identifiers & Regulatory

Product NDC 0781-2074

Product ID 0781-2074_1a70cb03-12cb-4708-a047-78d2d7db8fb6

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA074821

Listing Expiration 2026-12-31

Marketing Start 1997-06-05

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 07812074

Hyphenated Format 0781-2074

Supplemental Identifiers

RxCUI

198316

UNII

0J48LPH2TH WS821Z52LQ

NUI

N0000175359 N0000175419 M0471776 N0000008859 N0000175418

Packaging Origin

Original Packager

true

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 ANDA074821 (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

25 mg/1
37.5 mg/1

source: ndc

Packaging

100 CAPSULE in 1 BOTTLE (0781-2074-01)
1000 CAPSULE in 1 BOTTLE (0781-2074-10)

source: ndc

Packages (2)

0781-2074-01 100 CAPSULE in 1 BOTTLE (0781-2074-01) 0781-2074-10 1000 CAPSULE in 1 BOTTLE (0781-2074-10)

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": "1a70cb03-12cb-4708-a047-78d2d7db8fb6", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["198316"], "spl_set_id": ["f824b6ba-bd1c-41a8-8f6f-ad507b48f3e0"], "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": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (0781-2074-01)", "package_ndc": "0781-2074-01", "marketing_start_date": "19970605"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (0781-2074-10)", "package_ndc": "0781-2074-10", "marketing_start_date": "19970605"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "0781-2074_1a70cb03-12cb-4708-a047-78d2d7db8fb6", "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": "0781-2074", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Sandoz 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": "ANDA074821", "marketing_category": "ANDA", "marketing_start_date": "19970605", "listing_expiration_date": "20261231"}