spironolactone

Generic: spironolactone

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name spironolactone
Generic Name spironolactone
Labeler bryant ranch prepack
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

spironolactone 100 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0304
Product ID 71335-0304_d1dcd838-4b07-41ab-abf1-2a291210e39d
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 713350304
Hyphenated Format 71335-0304

Supplemental Identifiers

RxCUI
198222
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
  • 100 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (71335-0304-1)
  • 3 TABLET, FILM COATED in 1 BOTTLE (71335-0304-2)
  • 30 TABLET, FILM COATED in 1 BOTTLE (71335-0304-3)
  • 90 TABLET, FILM COATED in 1 BOTTLE (71335-0304-4)
  • 60 TABLET, FILM COATED in 1 BOTTLE (71335-0304-5)
source: ndc

Packages (5)

71335-0304-1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0304-1) 71335-0304-2 3 TABLET, FILM COATED in 1 BOTTLE (71335-0304-2) 71335-0304-3 30 TABLET, FILM COATED in 1 BOTTLE (71335-0304-3) 71335-0304-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-0304-4) 71335-0304-5 60 TABLET, FILM COATED in 1 BOTTLE (71335-0304-5)

Ingredients (1)

spironolactone (100 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": "d1dcd838-4b07-41ab-abf1-2a291210e39d", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["198222"], "spl_set_id": ["2ed347bc-a9f1-4800-99bc-9af9912ead1f"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71335-0304-1)", "package_ndc": "71335-0304-1", "marketing_start_date": "20220209"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE (71335-0304-2)", "package_ndc": "71335-0304-2", "marketing_start_date": "20220209"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-0304-3)", "package_ndc": "71335-0304-3", "marketing_start_date": "20220209"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-0304-4)", "package_ndc": "71335-0304-4", "marketing_start_date": "20220209"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71335-0304-5)", "package_ndc": "71335-0304-5", "marketing_start_date": "20220209"}], "brand_name": "Spironolactone", "product_id": "71335-0304_d1dcd838-4b07-41ab-abf1-2a291210e39d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "71335-0304", "generic_name": "spironolactone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "100 mg/1"}], "application_number": "ANDA203512", "marketing_category": "ANDA", "marketing_start_date": "20170602", "listing_expiration_date": "20261231"}