triamterene and hydrochlorothiazide (51655-582)

Drug Facts

Product Profile

Brand Name triamterene and hydrochlorothiazide

Generic Name triamterene and hydrochlorothiazide

Labeler northwind health company, llc

Dosage Form TABLET

Routes

ORAL

Active Ingredients

hydrochlorothiazide 50 mg/1, triamterene 75 mg/1

Manufacturer

Northwind Health Company, LLC

Identifiers & Regulatory

Product NDC 51655-582

Product ID 51655-582_494e6dd6-962e-2190-e063-6394a90a7ca5

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA071251

Listing Expiration 2027-12-31

Marketing Start 2022-12-30

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 51655582

Hyphenated Format 51655-582

Supplemental Identifiers

RxCUI

310818

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

50 mg/1
75 mg/1

source: ndc

Packaging

90 TABLET in 1 BOTTLE, PLASTIC (51655-582-26)
30 TABLET in 1 BOTTLE, PLASTIC (51655-582-52)

source: ndc

Packages (2)

51655-582-26 90 TABLET in 1 BOTTLE, PLASTIC (51655-582-26) 51655-582-52 30 TABLET in 1 BOTTLE, PLASTIC (51655-582-52)

Ingredients (2)

hydrochlorothiazide (50 mg/1) triamterene (75 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": "494e6dd6-962e-2190-e063-6394a90a7ca5", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310818"], "spl_set_id": ["f32b8809-80e9-18f2-e053-2995a90a5428"], "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": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (51655-582-26)", "package_ndc": "51655-582-26", "marketing_start_date": "20221230"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-582-52)", "package_ndc": "51655-582-52", "marketing_start_date": "20230103"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "51655-582_494e6dd6-962e-2190-e063-6394a90a7ca5", "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": "51655-582", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamterene and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}, {"name": "TRIAMTERENE", "strength": "75 mg/1"}], "application_number": "ANDA071251", "marketing_category": "ANDA", "marketing_start_date": "20221230", "listing_expiration_date": "20271231"}