triamterene and hydrochlorothiazide
Generic: triamterene and hydrochlorothiazide
Labeler: viona pharmaceuticals incDrug Facts
Product Profile
Brand Name
triamterene and hydrochlorothiazide
Generic Name
triamterene and hydrochlorothiazide
Labeler
viona pharmaceuticals inc
Dosage Form
CAPSULE
Routes
Active Ingredients
hydrochlorothiazide 25 mg/1, triamterene 37.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72578-090
Product ID
72578-090_ba702c00-5dc6-4545-bde9-ff7dbb7fd1a7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208358
Listing Expiration
2026-12-31
Marketing Start
2020-02-21
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72578090
Hyphenated Format
72578-090
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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
ANDA208358 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 37.5 mg/1
Packaging
- 100 CAPSULE in 1 BOTTLE (72578-090-01)
- 500 CAPSULE in 1 BOTTLE (72578-090-05)
- 1000 CAPSULE in 1 BOTTLE (72578-090-10)
- 10 BLISTER PACK in 1 CARTON (72578-090-77) / 10 CAPSULE in 1 BLISTER PACK (72578-090-30)
Packages (4)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ba702c00-5dc6-4545-bde9-ff7dbb7fd1a7", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["198316"], "spl_set_id": ["9925ab75-e3b7-43b7-888e-a2c8763240ba"], "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": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (72578-090-01)", "package_ndc": "72578-090-01", "marketing_start_date": "20200221"}, {"sample": false, "description": "500 CAPSULE in 1 BOTTLE (72578-090-05)", "package_ndc": "72578-090-05", "marketing_start_date": "20200221"}, {"sample": false, "description": "1000 CAPSULE in 1 BOTTLE (72578-090-10)", "package_ndc": "72578-090-10", "marketing_start_date": "20200221"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (72578-090-77) / 10 CAPSULE in 1 BLISTER PACK (72578-090-30)", "package_ndc": "72578-090-77", "marketing_start_date": "20200221"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "72578-090_ba702c00-5dc6-4545-bde9-ff7dbb7fd1a7", "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": "72578-090", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Viona Pharmaceuticals 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": "ANDA208358", "marketing_category": "ANDA", "marketing_start_date": "20200221", "listing_expiration_date": "20261231"}