FDA.reportPublic FDA data

NDC 51662-1264-02 - SOLU-MEDROL

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
51662-1264
Requested NDC
51662-1264-02
Package NDCs from labels
51662-1264-2, 51662-1264-3, 51662-1264-1, 51662-1264-02
Manufacturer
HF Acquisition Co. LLC, DBA HealthFirst
Effective date
2024-02-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
SOLU-MEDROL - HF Acquisition Co. LLC, DBA HealthFirstHF Acquisition Co. LLC, DBA HealthFirst2024-02-22HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51662-1264-12020-02-07C16284748780-19d75b9d0-90a9-f424-e053-dadaa90a57ceSOLU-MEDROL® 40MG PER VIAL 1mL ACT-O-VIAL®
51662-1264-12020-01-31C16284748780-19d75b9d0-90a9-f424-e053-dadaa90a57ceSOLU-MEDROL® 40MG PER VIAL 1mL ACT-O-VIAL®

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51662-1264-1SOLU-MEDROL1 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, FOR SOLUTION18
51662-1264-2SOLU-MEDROL1 mL in 1 POUCHINJECTION, POWDER, FOR SOLUTION18
51662-1264-3SOLU-MEDROL25 in 1 CASEINJECTION, POWDER, FOR SOLUTION258

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51662-1264SOLU-MEDROL INJECTION, POWDER, FOR SOLUTION [HF ACQUISITION CO. LLC, DBA HEALTHFIRST]8Current NDC, Legacy NDC, 3 package rows20240224_74e5060c-8426-1b77-e053-2a91aa0a1f13.zip

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 4 · 67 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Methylprednisolone Sodium SuccinateMETHYLPREDNISOLONE SODIUM SUCCINATEREMEDYREPACK INC.ae524bdb-9fd0-49f9-802d-465a374c175b2026-09-08Warnings, Adverse reactionsExact identifier
rxcui: 1743704
unii: LEC9GKY20K
Para-ChordHOMEOPATHIC LIQUIDEnergetix Corporation9f8f646e-634a-47ff-b208-b2249d685e552026-08-11WarningsExact identifier
unii: GR686LBA74
METHYLPREDNISOLONE SODIUM SUCCINATEMETHYLPREDNISOLONE SODIUM SUCCINATEHF Acquisition Co LLC, DBA HealthFirst559427ac-9fc6-96f5-e063-6294a90a0b302026-07-24Warnings, Adverse reactionsExact identifier
rxcui: 1743704
unii: LEC9GKY20K
SOLU-MEDROLMETHYLPREDNISOLONE SODIUM SUCCINATESportpharm LLC0cb0ba76-067f-46c4-a5d8-b585d5ecafe32026-07-23Warnings, Adverse reactionsExact identifier
application number: NDA011856
rxcui: 1743707
rxcui: 1743704
unii: LEC9GKY20K
Solu-MedrolMETHYLPREDNISOLONE SODIUM SUCCINATECardinal Health 107, LLC68ef8ec4-16de-4a8c-8696-b093596603802026-07-17Warnings, Adverse reactionsExact identifier
application number: NDA011856
rxcui: 1743707
rxcui: 1743704
unii: LEC9GKY20K
SOLU-MEDROLMETHYLPREDNISOLONE SODIUM SUCCINATEPharmacia & Upjohn Company LLC7271310c-7764-4812-aa30-a5e90987c7a92026-06-25Warnings, Adverse reactionsExact identifier
application number: NDA011856
ndc (product): 0009-0039
rxcui: 1743707
rxcui: 1743704
rxcui: 207191
rxcui: 207193
rxcui: 314099
rxcui: 311659
spl id: 9fdbd924-74fd-4b07-882c-d7e11b1a4642
spl set id: 7271310c-7764-4812-aa30-a5e90987c7a9
unii: LEC9GKY20K
Methylprednisolone Sodium SuccinateMETHYLPREDNISOLONE SODIUM SUCCINATEEugia US LLC2035f00e-2299-473a-b004-cb93f541cfa92026-06-12Warnings, Adverse reactionsExact identifier
rxcui: 1357886
rxcui: 1743704
rxcui: 314099
rxcui: 311659
unii: LEC9GKY20K
Solu-MedrolMETHYLPREDNISOLONE SODIUM SUCCINATEHenry Schein, Inc.ea2f9b6f-2375-40a6-8b97-b607b9f3ac632026-06-04Warnings, Adverse reactionsExact identifier
application number: NDA011856
rxcui: 1743707
rxcui: 1743704
unii: LEC9GKY20K
SOLU-MEDROLMETHYLPREDNISOLONE SODIUM SUCCINATEA-S Medication Solutions8e5997ed-f4a5-43f7-abbd-c8e2219fe0e92026-05-29Warnings, Adverse reactionsExact identifier
application number: NDA011856
rxcui: 1743707
rxcui: 1743704
unii: LEC9GKY20K
Solu-MedrolMETHYLPREDNISOLONE SODIUM SUCCINATECardinal Health 107, LLC2af28649-2553-4bcc-9cb1-c73f7cec76d52026-05-20Warnings, Adverse reactionsExact identifier
application number: NDA011856
rxcui: 1743707
rxcui: 1743704
rxcui: 207191
rxcui: 311659
unii: LEC9GKY20K
Methylprednisolone sodium succinateMETHYLPREDNISOLONE SODIUM SUCCINATEREMEDYREPACK INC.f339882f-c380-4022-bdcd-94556a7926aa2026-04-15Warnings, Adverse reactionsExact identifier
rxcui: 1743704
unii: LEC9GKY20K
Solu-MedrolMETHYLPREDNISOLONE SODIUM SUCCINATEHenry Schein, Inc.decceb81-e922-4b72-a278-3ed80f4adb042026-03-18Warnings, Adverse reactionsExact identifier
application number: NDA011856
rxcui: 207191
rxcui: 311659
unii: LEC9GKY20K
CVS PharmacySALINE LAXATIVECVS Pharmacyedd58c52-18de-4ec4-aec3-44f3e17607a72026-02-17WarningsExact identifier
unii: GR686LBA74
Methylprednisolone Sodium SuccinateMETHYLPREDNISOLONE SODIUM SUCCINATEHikma Pharmaceuticals USA Inc.060bcf13-ce9e-488c-ad43-9d66abb23b182026-02-17Warnings, Adverse reactionsExact identifier
rxcui: 314099
unii: LEC9GKY20K
Methylprednisolone Sodium SuccinateMETHYLPREDNISOLONE SODIUM SUCCINATECivica, Inc.2e6020f5-a486-41cc-8956-58b5f6751aa22026-02-17Warnings, Adverse reactionsExact identifier
rxcui: 1743704
rxcui: 311659
unii: LEC9GKY20K
Methylprednisolone Sodium SuccinateMETHYLPREDNISOLONE SODIUM SUCCINATEHikma Pharmaceuticals USA Inc.05d95a56-b03a-4d5b-9877-2853ac470fa12026-02-13Warnings, Adverse reactionsExact identifier
rxcui: 1743704
rxcui: 311659
unii: LEC9GKY20K
Methylprednisolone Sodium SuccinateMETHYLPREDNISOLONE SODIUM SUCCINATEHikma Pharmaceuticals USA Inc.2e540674-0915-4498-8e2b-751c7e97532a2026-02-13Warnings, Adverse reactionsExact identifier
rxcui: 314099
unii: LEC9GKY20K
SOLU-MEDROLMETHYLPREDNISOLONE SODIUM SUCCINATEREMEDYREPACK INC.1d5ef347-2e9a-432f-9a88-a7c4ba3002672026-01-30Warnings, Adverse reactionsExact identifier
application number: NDA011856
rxcui: 1743707
rxcui: 1743704
unii: LEC9GKY20K
Equate Ready-to-Use Enema LaxativeSODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMWalMart04c7440e-5b25-4b63-9604-321298d510212026-01-29WarningsExact identifier
unii: GR686LBA74
Quality Choice LaxativeSODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMChain Drug Marketing Association1cac3b6b-155b-47bb-bb79-17c55d3457362026-01-28WarningsExact identifier
unii: GR686LBA74

Reported adverse events (FAERS/openFDA)#

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