spironolactone

Generic: spironolactone

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name spironolactone
Generic Name spironolactone
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

spironolactone 50 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3795
Product ID 68071-3795_2e5e782d-9cec-d4a4-e063-6294a90aba3a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA202187
Listing Expiration 2026-12-31
Marketing Start 2019-12-13

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 680713795
Hyphenated Format 68071-3795

Supplemental Identifiers

RxCUI
198223
UPC
0368071379594
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 ANDA202187 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (68071-3795-9)
source: ndc

Packages (1)

68071-3795-9 90 TABLET in 1 BOTTLE (68071-3795-9)

Ingredients (1)

spironolactone (50 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": "2e5e782d-9cec-d4a4-e063-6294a90aba3a", "openfda": {"nui": ["N0000175557", "N0000011310"], "upc": ["0368071379594"], "unii": ["27O7W4T232"], "rxcui": ["198223"], "spl_set_id": ["2e5e782d-9ceb-d4a4-e063-6294a90aba3a"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3795-9)", "package_ndc": "68071-3795-9", "marketing_start_date": "20250217"}], "brand_name": "SPIRONOLACTONE", "product_id": "68071-3795_2e5e782d-9cec-d4a4-e063-6294a90aba3a", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "68071-3795", "generic_name": "SPIRONOLACTONE", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SPIRONOLACTONE", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "50 mg/1"}], "application_number": "ANDA202187", "marketing_category": "ANDA", "marketing_start_date": "20191213", "listing_expiration_date": "20261231"}