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XEOMIN 100 U Vial - SFDA Drug Approval Details
Approvals
/
SFDA
/
XEOMIN 100 U Vial
Authorized
BIOLOGICAL
XEOMIN 100 U Vial
Unknown
🇸🇦 Saudi Food and Drug Authority
Approval Date
N/A
Approval ID
4e72da21a419748e
Company
Unknown
Type
Biological
Approval Details
Approval Id
4e72da21a419748e
Drug Approval Sfda Name
XEOMIN 100 U Vial
Trade Name
XEOMIN 100 U Vial
Generic Name
CLOSTRIDIUM BOTULINUM NEUROTOXIN A
Register Number
1911246275
Register Year
2019
Drug Type
Biological
Route Of Administration
Intramuscular use
Package Type
Vial
Package Size
1
Legal Status
Prescription
Authorization Status
Valid
Marketing Status
Marketed
Product Control
Restricted
Storage Conditions
store below 25°c
Shelf Life
36 Months
Distribution Site
Hospital
Description Code
7000000614-100-100000073866
Price
647.9
Active Ingredients
Authorized
Quick Info
Agency
SFDA
Country
🇸🇦
Approval ID
4e72da21a419748e
Type
Biological
Back to SFDA Approvals