ZOMIG Film-coated tablet Ref.[50369] Active ingredients: Zolmitriptan

Source: Υπουργείο Υγείας (CY)  Revision Year: 2022  Publisher: C.G. Papaloisou Ltd, 35 Kilkis Avenue, 2234 Cyprus

Product name and form

Zomig 2.5 mg film-coated tablets.

Pharmaceutical Form

Film-coated tablet.

Round, biconvex, yellow film-coated tablets containing 2.5 mg of zolmitriptan. The tablets are intagliated with the letter ‘Z’ on one side.

Qualitative and quantitative composition

Zolmitriptan.

Each 2.5 mg film-coated tablet contains 2.5 mg zolmitriptan.

Excipients: Each 2.5 mg film-coated tablet contains 100 mg lactose.

For a full list of excipients, see section 6.1.

Active Ingredient Description
Zolmitriptan

Zolmitriptan has been demonstrated to be a selective agonist for the vascular human recombinant 5HT1B and 5HT1D receptor subtypes. Zolmitriptan is a high affinity 5HT1B/1D receptor agonist with modest affinity for 5HT1A receptors.

List of Excipients

Lactose anhydrate
Microcrystalline cellulose
Sodium starch glycollate (Type A)
Magnesium stearate
Hypromellose
Macrogol (400 and 8000)
Iron oxide (E172: yellow)
Titanium dioxide (E171)

Pack sizes and marketing

Tablets of 2.5 in blister packs, containing 3 or 6 tablets.

The blister strip is polyamide Al-PVC/Al.

Not all pack sizes may be marketed.

Marketing authorization holder

C.G. Papaloisou Ltd, 35 Kilkis Avenue, 2234 Cyprus

Marketing authorization dates and numbers

Zomig 2.5 mg: 17688

13 April 1998

Drugs

Drug Countries
ZOMIG Austria, Australia, Brazil, Canada, Cyprus, Germany, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Italy, Japan, Lithuania, Malta, Mexico, Netherlands, Singapore, United Kingdom, United States, South Africa

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