spironolactone and hydrochlorothiazide

Generic: spironolactone and hydrochlorothiazide

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name spironolactone and hydrochlorothiazide
Generic Name spironolactone and hydrochlorothiazide
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydrochlorothiazide 25 mg/1, spironolactone 25 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-1625
Product ID 72162-1625_64464364-6052-4c03-9819-56c38f91aa83
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089534
Listing Expiration 2026-12-31
Marketing Start 1987-07-02

Pharmacologic Class

Established (EPC)
thiazide diuretic [epc] aldosterone antagonist [epc]
Mechanism of Action
aldosterone antagonists [moa]
Chemical Structure
thiazides [cs]
Physiologic Effect
increased diuresis [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721621625
Hyphenated Format 72162-1625

Supplemental Identifiers

RxCUI
198224
UNII
0J48LPH2TH 27O7W4T232
NUI
N0000175359 N0000175419 M0471776 N0000175557 N0000011310

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 spironolactone and hydrochlorothiazide (source: ndc)
Generic Name spironolactone and hydrochlorothiazide (source: ndc)
Application Number ANDA089534 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1625-0)
  • 100 TABLET in 1 BOTTLE, PLASTIC (72162-1625-1)
  • 30 TABLET in 1 BOTTLE, PLASTIC (72162-1625-3)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1625-4)
  • 500 TABLET in 1 BOTTLE, PLASTIC (72162-1625-5)
  • 60 TABLET in 1 BOTTLE, PLASTIC (72162-1625-6)
source: ndc

Packages (6)

72162-1625-0 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1625-0) 72162-1625-1 100 TABLET in 1 BOTTLE, PLASTIC (72162-1625-1) 72162-1625-3 30 TABLET in 1 BOTTLE, PLASTIC (72162-1625-3) 72162-1625-4 1000 TABLET in 1 BOTTLE, PLASTIC (72162-1625-4) 72162-1625-5 500 TABLET in 1 BOTTLE, PLASTIC (72162-1625-5) 72162-1625-6 60 TABLET in 1 BOTTLE, PLASTIC (72162-1625-6)

Ingredients (2)

hydrochlorothiazide (25 mg/1) spironolactone (25 mg/1)

Linked Drug Pages (1)

Spironolactone and Hydrochlorothiazide ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "64464364-6052-4c03-9819-56c38f91aa83", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000175557", "N0000011310"], "unii": ["0J48LPH2TH", "27O7W4T232"], "rxcui": ["198224"], "spl_set_id": ["b3228678-7992-4148-b4ab-aa0d8b1b8570"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1625-0)", "package_ndc": "72162-1625-0", "marketing_start_date": "20230927"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1625-1)", "package_ndc": "72162-1625-1", "marketing_start_date": "20230927"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72162-1625-3)", "package_ndc": "72162-1625-3", "marketing_start_date": "20230927"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1625-4)", "package_ndc": "72162-1625-4", "marketing_start_date": "20230927"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72162-1625-5)", "package_ndc": "72162-1625-5", "marketing_start_date": "20230927"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (72162-1625-6)", "package_ndc": "72162-1625-6", "marketing_start_date": "20230927"}], "brand_name": "Spironolactone and Hydrochlorothiazide", "product_id": "72162-1625_64464364-6052-4c03-9819-56c38f91aa83", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "72162-1625", "generic_name": "Spironolactone and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA089534", "marketing_category": "ANDA", "marketing_start_date": "19870702", "listing_expiration_date": "20261231"}