COLDREX

500MG/25MG/5MG/20MG/30MG TBL NOB 14

SÚKL code 0162139
Name of the product COLDREX TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i COLDREX
Supplement 500MG/25MG/5MG/20MG/30MG TBL NOB 14
Strenght 500MG/25MG/5MG/20MG/30MG
Pharmaceutical form Tablet
Package 14
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status OTC medicinal products
Active substance CAFFEINE (COFFEINUM)
PARACETAMOL (PARACETAMOLUM)
PHENYLEPHRINE HYDROCHLORIDE (PHENYLEPHRINI HYDROCHLORIDUM)
TERPIN MONOHYDRATE (TERPINUM MONOHYDRICUM)
ASCORBIC ACID COATED WITH ETHYLCELLULOSE (ACIDUM ASCORBICUM ETHYLCELLULOSO OBDUCTUM)
ATC group N02BE51
ATC group name PARACETAMOL, KOMBINACE KROMĚ PSYCHOLEPTIK

Marketing authorisation information

Registration Number 07/ 180/92-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. 06. 2016
MA Holder GlaxoSmithKline Consumer Healthcare, GlaxoSmithKline Export Limited, Brentford
MA Holder country VELKÁ BRITÁNIE
Actual MA holder OMEGA PHARMA a.s., Brno
Actual MA holder country ČESKÁ REPUBLIKA

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