TENORET Film-coated tablet Ref.[28069] Active ingredients: Atenolol Chlortalidone

Source: Medicines & Healthcare Products Regulatory Agency (GB)  Revision Year: 2020  Publisher: AstraZeneca UK Limited., 600 Capability Green, Luton, LU1 3LU, UK

Product name and form

Tenoret 50 mg/12.5 mg film-coated tablets.

Pharmaceutical Form

Film-coated tablets.

White, round biconvex, film-coated, tablets which are intagliated with 50 12.5 on one face and bisected on the reverse face.

The score line is not intended for breaking the tablet.

Qualitative and quantitative composition

Atenolol 50 mg.

Chlortalidone 12.5 mg.

For the full list of excipients, see section 6.1.

Active Ingredient Description
Atenolol

Atenolol is a beta-blocker which is beta1-selective, (i.e. acts preferentially on beta1-adrenergic receptors in the heart). Atenolol is without intrinsic sympathomimetic and membrane-stabilising activities and as with other beta-blockers, has negative inotropic effects.

Chlortalidone

Chlortalidone is a benzothiadiazine (thiazide)-related diuretic with a long duration of action.

List of Excipients

Magnesium carbonate
Maize starch
Sodium laurilsulfate
Gelatin
Magnesium stearate
Methylhydroxypropylcellulose
Titanium dioxide
Glycerol (E422)

Pack sizes and marketing

Blister packs of 28 tablets contained in a carton.

Marketing authorization holder

AstraZeneca UK Limited., 600 Capability Green, Luton, LU1 3LU, UK

Marketing authorization dates and numbers

PL 17901/0048

Date of first authorisation: 01 June 2000
Date of latest renewal: 09 February 2005

Drugs

Drug Countries
TENORET Hong Kong, Nigeria, Singapore, United Kingdom, South Africa

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