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Blodis-1000 - Philippines FDA Drug Approval Details
Approvals
/
Philippines FDA
/
Blodis-1000
Approved
STANDARD
Blodis-1000
East African (India) Overseas
🇵🇭 Food and Drug Administration - Philippines
Approval Date
Jul 14, 2025
Approval ID
f67c53916b4adda9
Company
East African (India) Overseas
Type
Standard
Approval Details
Approval Id
f67c53916b4adda9
Drug Approval Philippines Name
Blodis-1000
Product Name
Blodis-1000
Registration Number
DRP-13202
Brand Name
Blodis-1000
Generic Name
Methylprednisolone (As Sodium Succinate)
Dosage Form
Lyophilized Powder for Injection (IM/IV)
Dosage Strength
1 g
Manufacturer
East African (India) Overseas
Importer
Ambica International Corporation.
Distributor
Ambica International Corporation.
Issuance Date
28 December 2022
Expiry Date
28 December 2027
Classification
Prescription Drug (RX)
Active Ingredients
Approved
Quick Info
Agency
Philippines FDA
Country
🇵🇭
Approval Date
Jul 14, 2025
Approval ID
f67c53916b4adda9
Type
Standard
Back to Philippines FDA Approvals