PANADOL ULTRA

500MG/8MG/30MG TBL NOB 12 I

SÚKL code 0208848
Name of the product PANADOL ULTRA
_MA_MEDICATION_DETAIL_INFO_MED_NAME i PANADOL ULTRA
Supplement 500MG/8MG/30MG TBL NOB 12 I
Strenght 500MG/8MG/30MG
Pharmaceutical form Tablet
Package 12 I
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance CAFFEINE (COFFEINUM)
PARACETAMOL (PARACETAMOLUM)
CODEINE PHOSPHATE HEMIHYDRATE (CODEINI PHOSPHAS HEMIHYDRICUS)
ATC group N02AJ06
ATC group name KODEIN A PARACETAMOL

Marketing authorisation information

Registration Number 07/ 300/98-C
Type of MA National
MA status R - active MA/authorised medicinal product
MA Holder GlaxoSmithKline Consumer Healthcare Czech Republic s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA

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