spironolactone

Generic: spironolactone

Labeler: asclemed usa, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name spironolactone
Generic Name spironolactone
Labeler asclemed usa, inc.
Dosage Form TABLET, COATED
Routes
ORAL
Active Ingredients

spironolactone 50 mg/1

Manufacturer
Asclemed USA, Inc.

Identifiers & Regulatory

Product NDC 76420-926
Product ID 76420-926_2fa991e8-8594-6911-e063-6294a90a916d
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA040750
Listing Expiration 2026-12-31
Marketing Start 2021-01-04

Pharmacologic Class

Established (EPC)
aldosterone antagonist [epc]
Mechanism of Action
aldosterone antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420926
Hyphenated Format 76420-926

Supplemental Identifiers

RxCUI
198222 198223 313096
UNII
27O7W4T232
NUI
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 (source: ndc)
Generic Name spironolactone (source: ndc)
Application Number ANDA040750 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 1000 TABLET, COATED in 1 BOTTLE (76420-926-00)
  • 100 TABLET, COATED in 1 BOTTLE (76420-926-01)
  • 500 TABLET, COATED in 1 BOTTLE (76420-926-05)
  • 30 TABLET, COATED in 1 BOTTLE (76420-926-30)
  • 60 TABLET, COATED in 1 BOTTLE (76420-926-60)
  • 90 TABLET, COATED in 1 BOTTLE (76420-926-90)
source: ndc

Packages (6)

Ingredients (1)

spironolactone (50 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2fa991e8-8594-6911-e063-6294a90a916d", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["db22e9e5-2d88-4712-a809-c00881edb447"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (76420-926-00)", "package_ndc": "76420-926-00", "marketing_start_date": "20250306"}, {"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (76420-926-01)", "package_ndc": "76420-926-01", "marketing_start_date": "20250306"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (76420-926-05)", "package_ndc": "76420-926-05", "marketing_start_date": "20250306"}, {"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (76420-926-30)", "package_ndc": "76420-926-30", "marketing_start_date": "20250306"}, {"sample": false, "description": "60 TABLET, COATED in 1 BOTTLE (76420-926-60)", "package_ndc": "76420-926-60", "marketing_start_date": "20250306"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (76420-926-90)", "package_ndc": "76420-926-90", "marketing_start_date": "20250306"}], "brand_name": "Spironolactone", "product_id": "76420-926_2fa991e8-8594-6911-e063-6294a90a916d", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "76420-926", "generic_name": "Spironolactone", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20210104", "listing_expiration_date": "20261231"}