NDC 83939-0022-01 - Oxybutynin Chloride

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
83939-0022
Requested NDC
83939-0022-01
Package NDCs from labels
83939-0022-1, 83939-0022-2, 83939-0022-3, 83939-0022-01
Manufacturer
VERITYRX, LLC
Effective date
2025-10-31
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Oxybutynin Chloride - VERITYRX, LLCVERITYRX, LLC2025-10-31HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83939-0022-1Oxybutynin Chloride1 in 1 POUCHTABLET11
83939-0022-2Oxybutynin Chloride1 in 1 POUCHTABLET11
83939-0022-2Oxybutynin Chloride50 in 1 BOX, UNIT-DOSETABLET501
83939-0022-3Oxybutynin Chloride1 in 1 POUCHTABLET11
83939-0022-3Oxybutynin Chloride100 in 1 BOX, UNIT-DOSETABLET1001

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 2 of 5 · 83 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Oxybutynin ChlorideOXYBUTYNIN CHLORIDECoupler LLC3f7dc283-b168-8251-e063-6294a90a45a22025-12-24Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDECoupler LLC3f7da2a3-ca46-d3e8-e063-6294a90abef32025-12-24Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
oxybutynin chlorideOXYBUTYNIN CHLORIDEChartwell RX, LLCe464c8dd-5222-4a6b-b7e9-ca608a403c6e2025-12-22Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
oxybutynin chlorideOXYBUTYNIN CHLORIDEAccord Healthcare, Inc.61496a1e-17bf-4f45-a20c-5bb98fe545ee2025-12-16Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin Chloride Extended ReleaseOXYBUTYNIN CHLORIDEAvKARE94471401-a516-0fe7-ec9c-447dd2bee9722025-12-16Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDEUpsher-Smith Laboratories, LLC3ee6835a-7a7d-49a9-8460-2f1dd270ead32025-12-11Warnings, Adverse reactionsExact identifier
rxcui: 863664
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDEAjanta Pharma USA Inc.95c2a144-ba0d-4011-ae0f-0e0ca876e8a82025-11-30Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDEOXYBUTYNIN CHLORIDEA-S Medication Solutions44990ed6-b8e7-40f5-b636-e848024ec6d82025-11-18Warnings, Adverse reactionsExact identifier
rxcui: 863664
unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDEOXYBUTYNIN CHLORIDEA-S Medication Solutions0697b3cf-b146-47c0-b5a5-5905ae8d1c972025-11-18Warnings, Adverse reactionsExact identifier
rxcui: 863664
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDEVERITYRX, LLC427b6ffb-3ff4-932f-e063-6394a90ae8b92025-10-31Warnings, Adverse reactionsExact identifier
application number: ANDA209823
ndc (package): 83939-0022-3
ndc (package): 83939-0022-2
ndc (package): 83939-0022-1
ndc (product): 83939-0022
ndc11 (package): 83939002201
rxcui: 863664
spl id: 427b8d8e-0187-6ba0-e063-6294a90ac52b
spl set id: 427b6ffb-3ff4-932f-e063-6394a90ae8b9
unii: L9F3D9RENQ
Oxybutynin Chloride Extended ReleaseOXYBUTYNIN CHLORIDEPD-Rx Pharmaceuticals, Inc.b5653b7e-1e3b-4da3-b3a2-33318f448c672025-10-20Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin Chloride Extended ReleaseOXYBUTYNIN CHLORIDEPD-Rx Pharmaceuticals, Inc.e466d963-469a-4b1c-87f9-2e3e1e9bdf3d2025-10-02Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDEMajor Pharmaceuticals7769ad3d-6228-4b2d-8f44-4efe990d3fad2025-09-19Warnings, Adverse reactionsExact identifier
application number: ANDA209823
rxcui: 863664
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDECardinal Health 107, LLC8455b543-81ce-4522-ae9b-8396f944945c2025-08-18Warnings, Adverse reactionsExact identifier
application number: ANDA209823
rxcui: 863664
unii: L9F3D9RENQ
OXYBUTYNIN CHLORIDEOXYBUTYNIN CHLORIDEPD-Rx Pharmaceuticals, Inc.8bd5dce0-d56a-4e64-8de7-e7cd7775526b2025-08-18Warnings, Adverse reactionsExact identifier
rxcui: 863664
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDEMajor Pharmaceuticals7688cce8-797d-454c-95fb-52689741582e2025-07-15Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin Chloride Extended ReleaseOXYBUTYNIN CHLORIDERising Pharma Holdings, Inc.ab431781-3183-4638-b656-f40a61f079402025-05-19Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDEAvKARE3418ca19-feb0-9821-e063-6394a90ae8192025-05-01Warnings, Adverse reactionsExact identifier
rxcui: 863664
unii: L9F3D9RENQ
Oxybutynin Chloride Extended ReleaseOXYBUTYNIN CHLORIDEAvPAK242b4766-bc2b-0073-d72d-1bf879bbee242025-04-17Warnings, Adverse reactionsExact identifier
unii: L9F3D9RENQ
Oxybutynin ChlorideOXYBUTYNIN CHLORIDEPD-Rx Pharmaceuticals, Inc.9c8ced4b-94de-4df8-bea3-b42b8846b7692025-03-12Warnings, Adverse reactionsExact identifier
rxcui: 863664
unii: L9F3D9RENQ

Reported adverse events (FAERS/openFDA)#

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