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ULTIVA 2MG VIAL(LYOPHILIZED) - SFDA Drug Approval Details
Approvals
/
SFDA
/
ULTIVA 2MG VIAL(LYOPHILIZED)
Authorized
NCE
ULTIVA 2MG VIAL(LYOPHILIZED)
Unknown
🇸🇦 Saudi Food and Drug Authority
Approval Date
N/A
Approval ID
27e9b4e3c38309ee
Company
Unknown
Type
NCE
Approval Details
Approval Id
27e9b4e3c38309ee
Drug Approval Sfda Name
ULTIVA 2MG VIAL(LYOPHILIZED)
Trade Name
ULTIVA 2MG VIAL(LYOPHILIZED)
Generic Name
REMIFENTANIL HYDROCHLORIDE
Register Number
42-887-19
Register Year
2019
Drug Type
NCE
Route Of Administration
Intravenous use
Package Type
Vial
Package Size
5
Legal Status
Prescription
Authorization Status
Valid
Marketing Status
Marketed
Product Control
Controlled
Storage Conditions
store below 25°c
Shelf Life
24 Months
Distribution Site
Hospital
Description Code
7000001094-2-100000074029
Price
155.5
Active Ingredients
Authorized
Quick Info
Agency
SFDA
Country
🇸🇦
Approval ID
27e9b4e3c38309ee
Type
NCE
Back to SFDA Approvals