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ELIGARD 7.5 MG POWDER FOR SOLUTION FOR INJECTION - SFDA Drug Approval Details
Approvals
/
SFDA
/
ELIGARD 7.5 MG POWDER FOR SOLUTION FOR INJECTION
Authorized
NCE
ELIGARD 7.5 MG POWDER FOR SOLUTION FOR INJECTION
Unknown
🇸🇦 Saudi Food and Drug Authority
Approval Date
N/A
Approval ID
69131d65cba2e2a3
Company
Unknown
Type
NCE
Approval Details
Approval Id
69131d65cba2e2a3
Drug Approval Sfda Name
ELIGARD 7.5 MG POWDER FOR SOLUTION FOR INJECTION
Trade Name
ELIGARD 7.5 MG POWDER FOR SOLUTION FOR INJECTION
Generic Name
LEUPRORELIN
Register Number
2504245205
Register Year
2016
Drug Type
NCE
Route Of Administration
Subcutaneous use
Package Type
Vial
Package Size
1
Legal Status
Prescription
Authorization Status
Valid
Marketing Status
Marketed
Product Control
Restricted
Storage Conditions
store in a refrigerator (2°c – 8°c)
Shelf Life
24 Months
Distribution Site
Hospital
Description Code
7000000746-7.5-100000073868
Price
313.9
Active Ingredients
Authorized
Quick Info
Agency
SFDA
Country
🇸🇦
Approval ID
69131d65cba2e2a3
Type
NCE
Back to SFDA Approvals
