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- 63025
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Brand name
Component
Registration owner
Indication
Interaction
Unwanted Effect
Swissmedic-# (5-digit)
Pharmacode
Swissmedic Registration
63025
Date of registration
16.12.2014
Company name
Sanofi-Aventis (Suisse) SA
Revision date
Valid until
Indication
Date of market entry
Index Therapeuticus (BSV)
01.99.
Revocation Date
Index Therapeuticus (Swissmedic)
01.99.
Information for professionals
IP
Seq.-No.
Product
Description
Galenic form
ATC-classification
01
Lemtrada 10 mg/ml
solution à diluer pour perfusion
Concentrate for infusion (Alemtuzumab 12mg / 1.2ml)
L04AA34
CI
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