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SPEDRA 50 mg Tablet - SFDA Drug Approval Details
Approvals
/
SFDA
/
SPEDRA 50 mg Tablet
Authorized
NCE
SPEDRA 50 mg Tablet
Unknown
🇸🇦 Saudi Food and Drug Authority
Approval Date
N/A
Approval ID
c74e60c34bc9119b
Company
Unknown
Type
NCE
Approval Details
Approval Id
c74e60c34bc9119b
Drug Approval Sfda Name
SPEDRA 50 mg Tablet
Trade Name
SPEDRA 50 mg Tablet
Generic Name
AVANAFIL
Register Number
0404233469
Register Year
2017
Drug Type
NCE
Route Of Administration
Oral use
Package Type
Blister
Package Size
4
Legal Status
Prescription
Authorization Status
Valid
Marketing Status
Marketed
Product Control
Uncontrolled
Storage Conditions
store below 25°c
Shelf Life
36 Months
Distribution Site
Pharmacy
Description Code
7000000105-50-100000073664
Price
54.5
Active Ingredients
Authorized
Quick Info
Agency
SFDA
Country
🇸🇦
Approval ID
c74e60c34bc9119b
Type
NCE
Back to SFDA Approvals