Veterinary medicines

Ivertin

Recall | Veterinary Medicines | 26/11/2019
"Richter Pharma AG" has informed its customers on November 22, 2019 that the below mentioned batch of "Ivertin" will be recalled due to a possible reduced content of Ivermectin, which results from a deficiency of the vials.
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Anaestamine

Recall | Veterinary Medicines | 26/03/2019
The marketing authorisation holder and its distribution partner informed their customers on March 25, 2019 that particles had been detected in individual batches.
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Tylan

Recall | Veterinary Medicines | 30/11/2018

The marketing authorization holder has informed its supplied customers in a letter dated 28.11.2018 that sterility cannot be guaranteed due to an…

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Norocarp

Recall | Veterinary Medicines | 28/11/2018

The marketing authorization holder and the distributor have informed their supplied customers by letter dated 28.11.2018 that due to a malfunction in…

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Animeloxan

Recall | Veterinary Medicines | 15/11/2018

The marketing authorization holder has informed its supplied customers in a letter dated 13.11.2018 that the above batch is being recalled as a…

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Doxapram-V

Recall | Veterinary Medicines | 14/11/2018

Richter Pharma AG" as distributor of the veterinary medicinal product "Doxapram-V", which is approved in Germany, has informed its customers that the…

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Osurnia

Recall | Veterinary Medicines | 11/10/2018

The marketing authorization holder has informed its supplied customers by letter dated 09/10/2018 that an atypical trend in the level of non-specified…

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Doxapram-V

Recall | Veterinary Medicines | 24/07/2018

Richter Pharma AG" as distributor of the veterinary medicinal product "Doxapram-V", which is approved in Germany, has informed its customers that…

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Osurnia

Safety warnings | Veterinary Medicines | 03/05/2018
Osurnia is indicated for the treatment of acute otitis externa and acute exacerbations of recurrent otitis externa caused by Staphylococcus pseudointermedius and Malassezia pachydermatis.
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Enzaprost T

Recall | Veterinary Medicines | 14/02/2018

The marketing authorization holder has informed its supplied customers in a letter dated 02.01.2018 that the affected batch is being recalled as a…

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