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Philippines FDA
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Solu-Cortef
Approved
STANDARD
Solu-Cortef
Pharmacia and Upjohn Company LLC
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
21da16f3f3ed0512
Company
Pharmacia and Upjohn Company LLC
Type
Standard
Approval Details
Approval Id
21da16f3f3ed0512
Drug Approval Philippines Name
Solu-Cortef
Product Name
Solu-Cortef
Registration Number
DRP-2129
Brand Name
Solu-Cortef
Generic Name
Hydrocortisone (as Sodium Succinate)
Dosage Form
Sterile Powder For Injection (Im/Iv)
Dosage Strength
250mg/2mL
Manufacturer
Pharmacia and Upjohn Company LLC
Importer
Pfizer, Inc.
Company Detail Path
/organization/pharmacia-and-upjohn-company-llc
Importer Detail Path
/organization/pfizer-inc-pleasant-prairie-wisconsin-united-states
Issuance Date
24 November 2022
Expiry Date
09 October 2027
Pharmacologic Category
Corticosteroids
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
21da16f3f3ed0512
Type
Standard
Back to Philippines FDA Approvals
Solu-Cortef - Philippines FDA Drug Approval Details