triamterene and hydrochlorothiazide
Generic: triamterene and hydrochlorothiazide
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
triamterene and hydrochlorothiazide
Generic Name
triamterene and hydrochlorothiazide
Labeler
a-s medication solutions
Dosage Form
CAPSULE
Routes
Active Ingredients
hydrochlorothiazide 25 mg/1, triamterene 37.5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-7437
Product ID
50090-7437_59f02578-c37e-408c-86fd-9522d09af558
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
500907437
Hyphenated Format
50090-7437
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
ANDA208358 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
- 37.5 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE (50090-7437-0)
- 100 CAPSULE in 1 BOTTLE (50090-7437-1)
- 90 CAPSULE in 1 BOTTLE (50090-7437-4)
Packages (3)
Ingredients (2)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "59f02578-c37e-408c-86fd-9522d09af558", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["198316"], "spl_set_id": ["8857b70b-861d-44f8-a671-78c06c83c029"], "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": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (50090-7437-0)", "package_ndc": "50090-7437-0", "marketing_start_date": "20241106"}, {"sample": false, "description": "100 CAPSULE in 1 BOTTLE (50090-7437-1)", "package_ndc": "50090-7437-1", "marketing_start_date": "20241106"}, {"sample": false, "description": "90 CAPSULE in 1 BOTTLE (50090-7437-4)", "package_ndc": "50090-7437-4", "marketing_start_date": "20241106"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "50090-7437_59f02578-c37e-408c-86fd-9522d09af558", "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": "50090-7437", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "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"}