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BOTOX

100SU INJ PLV SOL 1

SÚKL code 0200405
Name of the product BOTOX
_MA_MEDICATION_DETAIL_INFO_MED_NAME i BOTOX
Supplement 100SU INJ PLV SOL 1
Strenght 100SU
Pharmaceutical form Powder for solution for injection
Package 1
Route Intradermal/intramuscular use
Language of the pack Czech
Wrap type Vial
Legal status na lékařský předpis
Active substance BOTULINUM TOXIN TYPE A (TOXINUM BOTULINICUM TYPUS A)
ATC group M03AX01
ATC group name BOTULOTOXIN

Marketing authorisation information

Registration Number 63/ 568/93-C
Type of MA National
MA status B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till)
Placed on the market till 30. 04. 2023
MA Holder Allergan Pharmaceuticals Ireland, Westport
MA Holder country IRSKO
Actual MA holder AbbVie s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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