spironolactone

Generic: spironolactone

Labeler: jubilant cadista pharmacuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name spironolactone
Generic Name spironolactone
Labeler jubilant cadista pharmacuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

spironolactone 25 mg/1

Manufacturer
Jubilant Cadista Pharmacuticals Inc.

Identifiers & Regulatory

Product NDC 59746-216
Product ID 59746-216_7839b797-5078-4aab-93a5-6056e4b9cdd5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203253
Listing Expiration 2026-12-31
Marketing Start 2013-02-01

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 59746216
Hyphenated Format 59746-216

Supplemental Identifiers

RxCUI
198222 198223 313096
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 ANDA203253 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (59746-216-01)
  • 500 TABLET, FILM COATED in 1 BOTTLE (59746-216-05)
  • 1000 TABLET, FILM COATED in 1 BOTTLE (59746-216-10)
source: ndc

Packages (3)

Ingredients (1)

spironolactone (25 mg/1)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7839b797-5078-4aab-93a5-6056e4b9cdd5", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222", "198223", "313096"], "spl_set_id": ["a7510768-8a52-4230-6aa0-b0d92d82588f"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Jubilant Cadista Pharmacuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59746-216-01)", "package_ndc": "59746-216-01", "marketing_start_date": "20170404"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59746-216-05)", "package_ndc": "59746-216-05", "marketing_start_date": "20170404"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (59746-216-10)", "package_ndc": "59746-216-10", "marketing_start_date": "20170404"}], "brand_name": "Spironolactone", "product_id": "59746-216_7839b797-5078-4aab-93a5-6056e4b9cdd5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "59746-216", "generic_name": "spironolactone", "labeler_name": "Jubilant Cadista Pharmacuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA203253", "marketing_category": "ANDA", "marketing_start_date": "20130201", "listing_expiration_date": "20261231"}