spironolactone

Generic: spironolactone

Labeler: sun pharmaceutical industries, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name spironolactone
Generic Name spironolactone
Labeler sun pharmaceutical industries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

spironolactone 25 mg/1

Manufacturer
Sun Pharmaceutical Industries, Inc.

Identifiers & Regulatory

Product NDC 53489-143
Product ID 53489-143_d58f76e0-60c3-42ec-8375-128cd42485f1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA089424
Listing Expiration 2026-12-31
Marketing Start 1986-07-23

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 53489143
Hyphenated Format 53489-143

Supplemental Identifiers

RxCUI
198222 198223 313096
UPC
0353489143011 0353489329019
UNII
27O7W4T232
NUI
N0000175557 N0000011310

Packaging Origin

Original Packager
true

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 ANDA089424 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE, PLASTIC (53489-143-01)
  • 500 TABLET in 1 BOTTLE, PLASTIC (53489-143-05)
  • 1000 TABLET in 1 BOTTLE, PLASTIC (53489-143-10)
source: ndc

Packages (3)

53489-143-01 100 TABLET in 1 BOTTLE, PLASTIC (53489-143-01) 53489-143-05 500 TABLET in 1 BOTTLE, PLASTIC (53489-143-05) 53489-143-10 1000 TABLET in 1 BOTTLE, PLASTIC (53489-143-10)

Ingredients (1)

spironolactone (25 mg/1)

Linked Drug Pages (1)

SPIRONOLACTONE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "d58f76e0-60c3-42ec-8375-128cd42485f1", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0353489143011", "0353489329019"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["c23b6b9b-aec3-48a8-a518-76e4097f6479"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (53489-143-01)", "package_ndc": "53489-143-01", "marketing_start_date": "19860723"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (53489-143-05)", "package_ndc": "53489-143-05", "marketing_start_date": "19860723"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (53489-143-10)", "package_ndc": "53489-143-10", "marketing_start_date": "19960723"}], "brand_name": "SPIRONOLACTONE", "product_id": "53489-143_d58f76e0-60c3-42ec-8375-128cd42485f1", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "53489-143", "generic_name": "SPIRONOLACTONE", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA089424", "marketing_category": "ANDA", "marketing_start_date": "19860723", "listing_expiration_date": "20261231"}