spironolactone

Generic: spironolactone

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name spironolactone
Generic Name spironolactone
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

spironolactone 25 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-3747
Product ID 50090-3747_81a3f77c-3d85-408a-a642-afc7cee5c1a8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203512
Listing Expiration 2026-12-31
Marketing Start 2017-06-02

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 500903747
Hyphenated Format 50090-3747

Supplemental Identifiers

RxCUI
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 ANDA203512 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3747-0)
  • 30 TABLET, FILM COATED in 1 BOTTLE (50090-3747-1)
  • 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3747-6)
source: ndc

Packages (3)

50090-3747-0 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3747-0) 50090-3747-1 30 TABLET, FILM COATED in 1 BOTTLE (50090-3747-1) 50090-3747-6 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3747-6)

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": "81a3f77c-3d85-408a-a642-afc7cee5c1a8", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["791251af-d276-40fc-8c35-9d179b20e219"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3747-0)", "package_ndc": "50090-3747-0", "marketing_start_date": "20170602"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-3747-1)", "package_ndc": "50090-3747-1", "marketing_start_date": "20181030"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-3747-6)", "package_ndc": "50090-3747-6", "marketing_start_date": "20170602"}], "brand_name": "Spironolactone", "product_id": "50090-3747_81a3f77c-3d85-408a-a642-afc7cee5c1a8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "50090-3747", "generic_name": "spironolactone", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA203512", "marketing_category": "ANDA", "marketing_start_date": "20170602", "listing_expiration_date": "20261231"}