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wuk02/21d June 2021
Hypurin® Porcine Insulin
(INSULIN Ph Eur)
Supporting diabetic patient choice
Indication: Licensed for the treatment of insulin dependent diabetes mellitus
Hypurin® Porcine insulin is an animal-derived insulin (porcine, pork base) and Wockhardt are the only remaining manufacturer in the world.
Not all diabetic patients suit the same insulin type so we feel it is important to provide the choice for those patients who wish to use it (and view it as a lifeline).
Although you may only see a relatively small number of patients who choose to use porcine insulin in the UK, by continuing our commitment to supply Hypurin® Porcine insulin we are providing them with the important choice to do so.
Product Range
| Wockhardt Order Code | PIP Code | Product License (P/L) Number | EAN / GTIN Code | Product Name | Strength | Pack Size |
|---|---|---|---|---|---|---|
| FP1856 | 240-7633 | 29831/0118 | 5012727-901947 | Hypurin® Porcine 30/70 Mix Insulin | 100 units per ml | 10ml vial |
| FP2476 | 293-7472 | 29831/0119 | 5012727-904061 | Hypurin® Porcine 30/70 Mix Insulin | 100 units per ml | 5x3ml cartridges |
| FP1854 | 240-7625 | 29831/0121 | 5012727-901923 | Hypurin® Porcine Isophane Insulin | 100 units per ml | 10ml vial |
| FP2474 | 293-7480 | 29831/0122 | 5012727-904047 | Hypurin® Porcine Isophane Insulin | 100 units per ml | 5x3ml cartridges |
| FP1855 | 240-7609 | 29831/0126 | 5012727-901930 | Hypurin® Porcine Neutral Insulin | 100 units per ml | 10ml vial |
| FP2475 | 293-7464 | 29831/0124 | 5012727-904054 | Hypurin® Porcine Neutral Insulin | 100 units per ml | 5x3ml cartridges |
Autopen® Classic pen-injector device
Hypurin® Insulin Profiles of action
Resources
Download the prescribing information for Hypurin® Porcine insulin today
Our Hypurin® Product Range
To view the summary of Product Characteristics documents (SmPCs) for Hypurin® Porcine insulin please click below
For further information, or to order Hypurin® insulin from Wockhardt UK please contact us
or email us at Hypurin-insulin@wockhardt.co.uk
(including the reporting of suspected ADRs and side effects)
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