Source: Medicines & Healthcare Products Regulatory Agency (GB) Revision Year: 2018 Publisher: Merck Sharp & Dohme Limited, Hertford Road, Hoddesdon, Hertfordshire EN11 9BU, UK
FOSAMAX Once Weekly 70 mg tablets.
| Pharmaceutical Form |
|---|
|
Tablet. Oval white tablets, marked with an outline of a bone image on one side, and ‘31’ on the other. |
Each tablet contains 70 mg alendronic acid (as sodium trihydrate).
Excipients with known effect: Each tablet contains 113.4 mg lactose (as lactose anhydrous).
For the full list of excipients, see section 6.1.
| Active Ingredient |
|---|
|
Alendronic acid is a bisphosphonate that inhibits osteoclastic bone resorption with no direct effect on bone formation. The bone formed during treatment with alendronic acid is of normal quality. |
| List of Excipients |
|---|
|
Microcrystalline cellulose |
Aluminum/aluminum blisters in cartons containing 2, 4, 8, 12 or 40 tablets.
Not all pack sizes may be marketed.
Merck Sharp & Dohme Limited, Hertford Road, Hoddesdon, Hertfordshire EN11 9BU, UK
PL 00025/0399
10 November 2000/9 November 2005
| Drug | Countries | |
|---|---|---|
| FOSAMAX | Austria, Brazil, Canada, Germany, Spain, France, Hong Kong, Croatia, Ireland, Italy, Mexico, Netherlands, New Zealand, Romania, Singapore, Turkey, United Kingdom, United States, South Africa |
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