Atomoxetine - Neuraxpharm UK

This information is intended for use by healthcare professionals.

Atomoxetine

Atomoxetine

Therapeutic indications: Atomoxetine is indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD) in children of 6 years and older, in adolescents and in adults as part of a comprehensive treatment programme. Treatment must be initiated by a specialist in the treatment of ADHD, such as a paediatrician, child/adolescent psychiatrist, or psychiatrist. Diagnosis should be made according to current DSM criteria or the guidelines in ICD.

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ADVERSE EVENTS SHOULD BE REPORTED

Reporting forms and information can be found at https://yellowcard.mhra.gov.uk/.

Adverse events should also be reported to Neuraxpharm UK Ltd by:

  • Email: pv-uk@neuraxpharm.com
  • Phone number: +44 330 128 0919

Technical information

Pharmaceutical form

Capsule, hard.

Excipients / Ingredients

Capsules content: Pregelatinized maize starch Silica colloidal anhydrous Dimeticone (350) Capsule shell: Gelatin Sodium Lauryl Sulfate Titanium dioxide (E171) Indigo carmine (E132) Printing ink (black) Shellac Glaze-45% (20% Esterified) in Ethanol Iron Oxide Black (E172) Propylene Glycol

Active substance

Atomoxetine

Strengths, Pack size and Information


Strength
Pack size
Pharmaceutical form
PIP Code
SmPC
PiL
10 mg
28 Capsules
123-8229
18 mg
28 Capsules
123-8211
25 mg
28 Capsules
123-8203
40 mg
28 Capsules
123-8237
60 mg
28 Capsules
123-8245
80 mg
28 Capsules
123-8393
100 mg
28 Capsules
123-8385
10 mg
7 Capsules
123-8419
18 mg
7 Capsules
123-8427
25 mg
7 Capsules
123-8435
40 mg
7 Capsules
123-8401

PROFESSIONAL ACCESS

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Item code no. NXUK032218, Date of prep. March 2022

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