Source: Medicines & Healthcare Products Regulatory Agency (GB) Revision Year: 2018 Publisher: Amdipharm UK Limited, Capital House, 85 King William Street, London EC4N 7BL, UK
Maxolon 10mg Tablets.
| Pharmaceutical Form |
|---|
|
White to ivory-white circular double convex tablet with a single break bar on one side. |
Each tablet contains Metoclopramide Hydrochloride BP 10mg equivalent to 10mg of the anhydrous substance.
Excipients with known effect:
Lactose: contains 125.00 mg of lactose per tablet.
For the full list of excipients, see section 6.1.
| Active Ingredient | Description | |
|---|---|---|
| Metoclopramide |
The action of metoclopramide is closely associated with parasympathetic nervous control of the upper gastro-intestinal tract where it has the effect of encouraging normal peristaltic action. This provides for a fundamental approach to the control of those conditions where disturbed gastrointestinal motility is a common underlying factor. |
| List of Excipients |
|---|
|
Maize starch (dried) |
Standard aluminium containers of 3, 6, 9, 12, 100 or 500 tablets.
Plastic reclosable containers packed into carton of 42, 84, 100 or 500 tablets.
Amber glass bottles of 100 or 500 tablets.
PVC blister (300 microns) of 20, 21, 42 or 84 tablets backed with aluminium foil (20 microns). The underside of the foils is coated with vinyl based laquer.
PVC (200 microns)/PVDC (60gsm) blister of 20, 21, 42 or 84 tablets.
Standard aluminium canister for 12 tablets packed with one ampoule of Maxolon injection as a home visit pack.
Not all pack sizes may be marketed.
Amdipharm UK Limited, Capital House, 85 King William Street, London EC4N 7BL, UK
PL 20072/0048
16 June 1995
| Drug | Countries | |
|---|---|---|
| MAXOLON | Australia, Ireland, New Zealand, United Kingdom, South Africa |
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