FDA.reportPublic FDA data

X

Manufacturer
AX Pharmaceutical Corp
Effective date
2015-12-13
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:48:10

Label at a glance#

ProductX
Active ingredientPREDNISOLONE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

copy of labelcopy of label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
b3fecff3-fb51-4f66-b443-a130905bb500Product name120250804
3a7a0034-a88d-88c3-f43e-ea34c6a216deProduct name220250311
9dbc4744-f7be-4393-b71a-e1bfd8b97659Product name220250218
9e44d9f9-cb87-3b0f-4c71-c8438d0dc2e5Product name220240102
a0e37fa3-7f16-4fbf-bdb7-ae82cb1a553aProduct name120170309
af7d3306-1338-423f-839e-419aad9e8a86Product name120170309
18d57d04-4a34-a130-5dd5-b7fc47f3b567Product name120140508
379bc253-901a-e6e1-92b7-0fc574249e07Product name120140508
48b05f5d-d2fc-45ab-76e8-3cb5bd44890dProduct name120140508
73adedd8-aba8-27d9-78d9-2e3c4a3cf954Product name120140508
9ae74339-0a3d-82e9-5dd1-88bd2607bd6bProduct name120140508
9f10552a-9a7b-8e6c-3223-dc44310af6cfProduct name120140508
e44e38a9-2d9e-b0e2-cce9-490554639f3dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62157-152-01X250 g in 1 BOTTLEPOWDER2501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62157-152X (PREDNISOLONE) POWDER [ AX PHARMACEUTICAL CORP]11 package rows20151214_dff7a6b0-2f7a-40d4-8ec7-816fd0ca1b0e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62157-15262157-152-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
PREDNISOLONE9PHQ9Y1OLMACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

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 1 of 1 · 7 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PrednisolonePREDNISOLONEA-S Medication Solutions35f0b197-c3ae-445a-8da7-9ffcd4472e052026-01-23Warnings, Adverse reactionsName fallback
generic name: PREDNISOLONE
PREDNISOLONEPREDNISOLONEZhejiang Xianju Pharmaceutical Co., Ltd.52e6e21d-94b8-41a0-8d13-371c0e66bcee2026-01-05Warnings, Adverse reactionsName fallback
generic name: PREDNISOLONE
PrednisolonePREDNISOLONEPAI Holdings, LLC dba PAI Pharmacebd7b5b-8e9f-4de9-9fcf-8ee0661fede32024-08-19Warnings, Adverse reactionsName fallback
generic name: PREDNISOLONE
PREDNISOLONEPREDNISOLONEHisun Pharmaceuticals USA, Inc.16d4e064-66d3-4497-8c7d-3aa355f91e1d2024-08-15Warnings, Adverse reactionsName fallback
generic name: PREDNISOLONE
PrednisolonePREDNISOLONEChartwell RX, LLC2e965355-f7f2-4dd3-9c5c-1524c6f39c912024-06-17Warnings, Adverse reactionsName fallback
generic name: PREDNISOLONE
PREDNISOLONEPREDNISOLONEAurobindo Pharma Limited070f1937-50a5-457f-bef5-4e597014e26d2024-02-16Warnings, Adverse reactionsName fallback
generic name: PREDNISOLONE
PrednisoLONEPREDNISOLONELannett Company, Inc.86652e2d-664a-4388-a611-c2a9aa4a4bc82024-02-14Warnings, Adverse reactionsName fallback
generic name: PREDNISOLONE

Reported adverse events (FAERS/openFDA)#

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