FDA.reportPublic FDA data

NDC 55154-3942-05 - Solu-Cortef

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
55154-3942
Requested NDC
55154-3942-05
Package NDCs from labels
55154-3942-5, 55154-3942-05
Manufacturer
Cardinal Health 107, LLC
Effective date
2025-08-21
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Solu-Cortef - Cardinal Health 107, LLCCardinal Health 107, LLC2025-08-21HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55154-3942-5Solu-Cortef5 in 1 BAGINJECTION, POWDER, FOR SOLUTION516
55154-3942-5Solu-Cortef2 mL in 1 VIAL, SINGLE-DOSEINJECTION, POWDER, FOR SOLUTION216

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55154-3942SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH 107, LLC]15Current NDC, Legacy NDC, 2 package rows20250112_f5bb0854-a477-4e59-914b-eeeaef92a596.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
55154-3942-5EA - Each55154-39428341a761-a60d-4db8-85cc-4e7a7c95305612019-05-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
hydrocortisone sodium succinateACTIVE INGREDIENT50LQB69S1ZSOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH]6
hydrocortisoneACTIVE MOIETYWI4X0X7BPJSOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH]6
benzyl alcoholINACTIVE INGREDIENTLKG8494WBHSOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH]6
sodium phosphate, dibasicINACTIVE INGREDIENTGR686LBA74SOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH]6
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUSINACTIVE INGREDIENTKH7I04HPUUSOLU-CORTEF (HYDROCORTISONE SODIUM SUCCINATE) INJECTION, POWDER, FOR SOLUTION [CARDINAL HEALTH]6

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 3 · 46 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Solu-CortefHYDROCORTISONE SODIUM SUCCINATEPharmacia & Upjohn Company LLC65eefd58-b166-4d71-ade6-45c8fdf869222026-08-27Warnings, Adverse reactionsExact identifier
application number: NDA009866
ndc (product): 0009-0011
rxcui: 105398
rxcui: 1738592
rxcui: 1738589
rxcui: 1738586
rxcui: 1738596
rxcui: 238755
rxcui: 1738594
rxcui: 1738590
spl id: 4e9814fe-3089-4980-a207-bf0aa95d4c36
spl set id: 65eefd58-b166-4d71-ade6-45c8fdf86922
unii: 50LQB69S1Z
Para-ChordHOMEOPATHIC LIQUIDEnergetix Corporation9f8f646e-634a-47ff-b208-b2249d685e552026-08-11WarningsExact identifier
unii: GR686LBA74
Hydrocortisone sodium succinateHYDROCORTISONE SODIUM SUCCINATEApotex Corp.bfe185a6-b657-2fbb-4ac2-e085373f15f32026-07-28Warnings, Adverse reactionsExact identifier
rxcui: 238755
unii: 50LQB69S1Z
Hydrocortisone sodium succinateHYDROCORTISONE SODIUM SUCCINATEZydus Lifesciences Limitedd533ebee-9f1c-42d7-9808-ae5d5e55741b2026-05-08Exact identifier
rxcui: 238755
unii: 50LQB69S1Z
Hydrocortisone sodium succinateHYDROCORTISONE SODIUM SUCCINATEZydus Pharmaceuticals USA Inc.37534164-9de5-4bb3-9f87-341dfcf908832026-05-08Warnings, Adverse reactionsExact identifier
rxcui: 238755
unii: 50LQB69S1Z
CVS PharmacySALINE LAXATIVECVS Pharmacyedd58c52-18de-4ec4-aec3-44f3e17607a72026-02-17WarningsExact identifier
unii: GR686LBA74
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
Sunmark Saline Single LaxativeSODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMStrategic Sourcing Services LLC06720229-7d58-499e-b7de-cb4bda5ae4162026-01-08WarningsExact identifier
unii: GR686LBA74
HealthMart Saline Single LaxativeSODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMStrategic Sourcing Services LLC689228de-1f3e-4205-853d-6004d62488572026-01-08WarningsExact identifier
unii: GR686LBA74
Uro-MPMETHENAMINE, SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS, PHENYL SALICYLATE, METHYLENE BLUE AND HYOSCYAMINE SULFATEMethod Pharmaceuticals, LLC1e1b0dee-1a3b-4846-a212-c9febb3fc17d2025-10-29Warnings, Adverse reactionsExact identifier
unii: KH7I04HPUU
Leader Ready to Use Saline LaxativeSODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMCardinal Health1b4f9c28-0547-4922-aa15-990c6fd9dc9f2025-09-29WarningsExact identifier
unii: GR686LBA74
Saline LaxativeSALINE LAXATIVEMajor Pharmaceuticalsb3758ffe-1bac-4df6-9714-5e33e9d28d902025-09-16WarningsExact identifier
unii: GR686LBA74
Solu-CortefHYDROCORTISONE SODIUM SUCCINATECardinal Health 107, LLCf5bb0854-a477-4e59-914b-eeeaef92a5962025-08-21Warnings, Adverse reactionsExact identifier
application number: NDA009866
ndc (package): 55154-3942-5
ndc (product): 55154-3942
ndc11 (package): 55154394205
rxcui: 105398
rxcui: 238755
spl id: bc348e8f-69c8-4cf4-a685-324ee3ebde87
spl set id: f5bb0854-a477-4e59-914b-eeeaef92a596
unii: 50LQB69S1Z
Solu-CortefHYDROCORTISONE SODIUM SUCCINATEProPharma Distribution386942d3-c75f-25f1-e063-6394a90a5af22025-07-18Warnings, Adverse reactionsExact identifier
application number: NDA009866
rxcui: 105398
rxcui: 238755
unii: 50LQB69S1Z
Rexall Ready to use 4pk LAXATIVESODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORMDolgencorp, LLC78509915-0ef1-4238-99a5-78a49a68f98f2025-07-07WarningsExact identifier
unii: GR686LBA74
InterSolPLATELET ADDITIVE 3Fenwal, Inc.17dec820-1b57-4ac9-82a8-419cab664a2f2025-06-27Warnings, Adverse reactionsExact identifier
unii: GR686LBA74
Saline LaxativeSODIUM PHOSPHATEWalgreen Companyfb260df0-7bda-4299-84a5-44c8f94477982025-06-18WarningsExact identifier
unii: GR686LBA74
PRISMASOL BGK2/0MAGNESIUM CHLORIDE, DEXTROSE ANHYDROUS, LACTIC ACID, SODIUM CHLORIDE, SODIUM BICARBONATE, AND POTASSIUM CHLORIDEVantive US Healthcare LLC7f675fee-8940-4ece-bb0c-75ac79d8708c2025-05-31Warnings, Adverse reactionsExact identifier
unii: GR686LBA74
Saline EnemaSODIUM PHOSPHATE MONOBASIC, SODIUM PHOSPHATE DIBASICDynarex Corporation7c7b68af-4ef2-4f84-9279-9f7a91c8d9c52025-05-14WarningsExact identifier
unii: GR686LBA74

Reported adverse events (FAERS/openFDA)#

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