triamterene and hydrochlorothiazide
Generic: triamterene and hydrochlorothiazide
Labeler: aphena pharma solutions - tennessee, llcDrug Facts
Product Profile
Brand Name
triamterene and hydrochlorothiazide
Generic Name
triamterene and hydrochlorothiazide
Labeler
aphena pharma solutions - tennessee, llc
Dosage Form
TABLET
Routes
Active Ingredients
hydrochlorothiazide 25 mg/1, triamterene 37.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71610-605
Product ID
71610-605_be54582f-c05d-4e2f-87fc-56bf6098f410
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071251
Listing Expiration
2026-12-31
Marketing Start
2009-09-21
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71610605
Hyphenated Format
71610-605
Supplemental Identifiers
RxCUI
UNII
NUI
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
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 37.5 mg/1
Packaging
- 90 TABLET in 1 BOTTLE (71610-605-60)
Packages (1)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "be54582f-c05d-4e2f-87fc-56bf6098f410", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812"], "spl_set_id": ["b129e54a-a6d8-42c0-baac-e8db2487369b"], "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": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71610-605-60)", "package_ndc": "71610-605-60", "marketing_start_date": "20211019"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "71610-605_be54582f-c05d-4e2f-87fc-56bf6098f410", "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": "71610-605", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "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": "20261231"}