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Last Updated: March 19, 2026

Details for New Drug Application (NDA): 009866


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NDA 009866 describes SOLU-CORTEF, which is a drug marketed by Pharmacia And Upjohn and is included in one NDA. It is available from four suppliers. Additional details are available on the SOLU-CORTEF profile page.

The generic ingredient in SOLU-CORTEF is hydrocortisone sodium succinate. There are sixty-seven drug master file entries for this compound. Five suppliers are listed for this compound. Additional details are available on the hydrocortisone sodium succinate profile page.
Summary for 009866
Tradename:SOLU-CORTEF
Applicant:Pharmacia And Upjohn
Ingredient:hydrocortisone sodium succinate
Patents:0
Pharmacology for NDA: 009866
Mechanism of ActionCorticosteroid Hormone Receptor Agonists
Suppliers and Packaging for NDA: 009866
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
SOLU-CORTEF hydrocortisone sodium succinate INJECTABLE;INJECTION 009866 NDA Pharmacia & Upjohn Company LLC 0009-0005 0009-0005-01 1 VIAL, SINGLE-DOSE in 1 CARTON (0009-0005-01) / 8 mL in 1 VIAL, SINGLE-DOSE
SOLU-CORTEF hydrocortisone sodium succinate INJECTABLE;INJECTION 009866 NDA Pharmacia & Upjohn Company LLC 0009-0011 0009-0011-04 25 VIAL, SINGLE-DOSE in 1 CARTON (0009-0011-04) / 2 mL in 1 VIAL, SINGLE-DOSE (0009-0011-03)

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 100MG BASE/VIAL
Approval Date:Approved Prior to Jan 1, 1982TE:APRLD:Yes

Profile for product number 002

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 250MG BASE/VIAL
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:Yes

Profile for product number 003

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrengthEQ 500MG BASE/VIAL
Approval Date:Approved Prior to Jan 1, 1982TE:RLD:Yes

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Preferred Citation:

Friedman, Yali. "DrugPatentWatch" DrugPatentWatch, thinkBiotech, 2026, www.DrugPatentWatch.com.
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