MedPath

ULTRA-TECHNEKOW FM 2,15-43,00 GBQ GENERADOR DE RADIONÚCLIDO

ULTRA-TECHNEKOW FM 2,15-43,00 GBQ GENERADOR DE RADIONÚCLIDO

Commercialized
Register Number

66374

Prescription Type

Uso Hospitalario

Authorization Date

Sep 28, 2004

Dosage Form

GENERADOR DE RADIONÚCLIDO

Route: VÍA INTRAVENOSA

Product Details

Detailed information about this CIMA AEMPS approved pharmaceutical product.

Basic Information

Key regulatory and product classification details

Regulatory Details

Register Number66374
EMA Approved
No

Drug Classification

Generic
Yes
Orphan
No
Biosimilar
No
Commercialized
Yes
CIMA AEMPS Classification

INGREDIENTS (2)

PERTECNETATO 99MTC SODIOActive
Quantity: 2,08-41,58 GBq
Name: PERTECNETATO 99MTC SODIO
SODIO MOLIBDATOActive
Quantity: 2,15-43,00 GBq
Name: SODIO MOLIBDATO

ATC CLASSIFICATION (3)

V09F
V09FX
V09FX01

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.