FDA.reportPublic FDA data

NDC 72162-1624-01 - SPIRONOLACTONE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
72162-1624
Requested NDC
72162-1624-01
Package NDCs from labels
72162-1624-0, 72162-1624-1, 72162-1624-3, 72162-1624-5, 72162-1624-6, 72162-1624-9, 72162-1624-01
Manufacturer
Bryant Ranch Prepack
Effective date
2026-03-30
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SPIRONOLACTONE - Bryant Ranch PrepackBryant Ranch Prepack2026-03-30HUMAN PRESCRIPTION DRUG LABEL
SPIRONOLACTONE - Aphena Pharma Solutions - Tennessee, LLCAphena Pharma Solutions - Tennessee, LLC2025-12-17HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72162-1624-0SPIRONOLACTONE1000 in 1 BOTTLETABLET1000109
72162-1624-1SPIRONOLACTONE100 in 1 BOTTLETABLET100109
72162-1624-3SPIRONOLACTONE30 in 1 BOTTLETABLET30109
72162-1624-5SPIRONOLACTONE500 in 1 BOTTLETABLET500109
72162-1624-6SPIRONOLACTONE60 in 1 BOTTLETABLET60109
72162-1624-9SPIRONOLACTONE90 in 1 BOTTLETABLET90109

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
72162-1624SPIRONOLACTONE TABLET [BRYANT RANCH PREPACK]108Current NDC, 6 package rows20250313_3791d79c-d960-4790-b689-ea32ddf7226a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72162-1624-0EA - Each72162-162434b5f845-d3a5-4201-896c-c73588c47ac712025-05-14
72162-1624-1EA - Each72162-162478c7cae0-2b4e-460b-9ee2-b656d9ff70e612023-07-06
72162-1624-3EA - Each72162-16244b6fd20b-e72c-427e-a885-6f56a62abd0612024-01-04
72162-1624-5EA - Each72162-16247bcf5f56-f2e1-4fb5-b222-91784fd75fcf12024-10-04
72162-1624-6EA - Each72162-1624b437eb85-1aed-4bfd-a90f-51a1de6a35a812024-01-04
72162-1624-9EA - Each72162-1624e3032663-7f96-4db7-af35-45c81aa766ae12024-10-04

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 5 of 57 · 1,133 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Docusate Sodium - Stool Softener LaxativeDOCUSATE SODIUMCardinal Health 107, LLCb5e4b14d-bf11-4309-bf6d-65ee9d877a242026-07-28WarningsExact identifier
unii: F05Q2T2JA0
GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPSPOLYVINYL ALCOHOL, POVIDONEAmerisourceBergence6852a8-c5e6-403d-a7b4-a2e85d1ebb1f2026-07-22WarningsExact identifier
unii: FZ989GH94E
Stool Softener LaxativeDOCUSATE SODIUMBryant Ranch Prepackdeca083b-5c72-40fa-9021-b74028426a5a2026-07-20WarningsExact identifier
unii: F05Q2T2JA0
Docusate SodiumDOCUSATE SODIUMCardinal Health 107, LLCfc5e82b6-e25c-4686-9781-2205819685f52026-07-20WarningsExact identifier
unii: F05Q2T2JA0
SpironolactoneSPIRONOLACTONEPD-Rx Pharmaceuticals, Inc.73564b3d-8ede-4008-b75c-1277153b5bb62026-07-17Warnings, Adverse reactionsExact identifier
rxcui: 313096
unii: 27O7W4T232
SpironolactoneSPIRONOLACTONEPD-Rx Pharmaceuticals, Inc.8a66d90e-5450-4716-8c01-e7dc1967d00d2026-07-17Warnings, Adverse reactionsExact identifier
rxcui: 198223
unii: 27O7W4T232
SpironolactoneSPIRONOLACTONEPD-Rx Pharmaceuticals, Inc.8cbe2215-744c-438a-b3d6-b7d6ae7692312026-07-17Warnings, Adverse reactionsExact identifier
rxcui: 198222
unii: 27O7W4T232
PridICHTHAMMOL, CALCIUM SULFIDE, CALENDULA OFFICINALIS FLOWERING TOP, ARNICA MONTANA, ECHINACEA ANGUSTIFOLIA, SILICON DIOXIDE, SULFURHyland's Inc.49689eeb-7790-07f1-e063-6294a90a2df22026-07-16WarningsExact identifier
unii: ETJ7Z6XBU4
stool softenerDOCUSATE SODIUMAmazon.com Services LLC4f83953e-3779-43b7-a5c6-7442a0675d9b2026-07-16WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener Extra StrengthDOCUSATE SODIUMDolgencorp, Inc. (DOLLAR GENERAL & REXALL)183576bd-c252-471b-8797-32cac5b0329c2026-07-16WarningsExact identifier
unii: F05Q2T2JA0
Stool SoftenerDOCUSATE SODIUMWalgreens3f9d54d9-a9d5-40ff-a8a2-431997b589992026-07-16WarningsExact identifier
unii: F05Q2T2JA0
Stool Softener LaxativeDOCUSATE SODIUMWalgreens7174021b-bdc0-4fd3-90e7-3904980033c42026-07-16WarningsExact identifier
unii: F05Q2T2JA0
SPIRONOLACTONESPIRONOLACTONEBryant Ranch Prepackbe4aa233-1555-4972-858e-46343a7105582026-07-16Warnings, Adverse reactionsExact identifier
application number: ANDA089424
rxcui: 198223
unii: 27O7W4T232
Stool SoftenerDOCUSATE SODIUMSTRATEGIC SOURCING SERVICES LLCff2179bd-cc76-9ee9-e053-6294a90a01c92026-07-15WarningsExact identifier
unii: F05Q2T2JA0
FEVIA Constipation ControlDOCUSATE SODIUMVIVUNT PHARMA LLC4b21ca11-b81f-402c-e063-6394a90a3acb2026-07-15WarningsExact identifier
unii: F05Q2T2JA0
Leg Cramps PMOYSTER SHELL CALCIUM CARBONATE, CRUDE, CAUSTICUM, MATRICARIA RECUTITA, CINCHONA OFFICINALIS BARK, COPPER, LYCOPODIUM CLAVATUM SPORE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, TOXICODENDRON PUBESCENS LEAF, SILICON DIOXIDE, AND SULFURHyland's Inc.b0574a7e-88fa-417e-b6d5-60ced59eba472026-07-15WarningsExact identifier
unii: ETJ7Z6XBU4
SPIRONOLACTONESPIRONOLACTONEBryant Ranch Prepack11d06acd-1351-4afd-a16a-f035758e2a272026-07-15Warnings, Adverse reactionsExact identifier
application number: ANDA089424
rxcui: 313096
unii: 27O7W4T232
Stool Softener LaxativeDOCUSATE SODIUM, SENNOSIDESWALMART INC. (see also Equate)43fd4231-0962-4828-a3fa-a1faec81e43d2026-07-15WarningsExact identifier
unii: F05Q2T2JA0
SPIRONOLACTONESPIRONOLACTONEBryant Ranch Prepackca194a2a-ed16-40f6-a78c-45c5f33921702026-07-15Warnings, Adverse reactionsExact identifier
application number: ANDA089424
rxcui: 313096
unii: 27O7W4T232
SPIRONOLACTONESPIRONOLACTONEBryant Ranch Prepackebc4efec-7895-4298-8e75-360bb7992f8d2026-07-15Warnings, Adverse reactionsExact identifier
application number: ANDA089424
rxcui: 313096
unii: 27O7W4T232

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.