for subcutaneous use Initial U.S. Approval: 2017
Facts about guselkumab injection
MEDICINE APPROVED BY-European Medical Agency (EMA), Food and Drug Administration (FDA), Health Canada, Pharmaceuticals and Medical Devices Agency (PMDA), Therapeutic Goods Administration (TGA)
Summary of FDA-approved use on approval date: Click Here
(see Drugs@FDA for complete indication)
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If you have a prescription from a Registered Medical Practitioner (RMP), IPN in Delhi can assist you in obtaining access to genuine medication. Our professional will provide you with a step-by-step guide on how to legally and safely import “guselkumab injection” based on the information you provide.
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Query For guselkumab injection
Approved accessible "guselkumab injection"
Guselkumab, sold under the brand name Tremfya, is a monoclonal antibody against interleukin-23 used for the treatment of plaque psoriasis. Guselkumab is indicated to treat moderate to severe plaque psoriasis, and psoriatic arthritis in adults. Guselkumab is provided as a subcutaneous injection of 100 mg given every eight weeks (except for the second dose, which is given four weeks after the first dose)
How can 1 go about obtaining guselkumab injection?
If guselkumab injection are not yet approved or available in your area, you may request its price in India under a specific brand name through IPN. For assistance and guidance, you can contact us by providing complete details. Our pharmaceutical expert will help you find a suitable and practical solution to your query. To receive comprehensive support, please call us at +91 9891 296 838 (Mr. Tarun) / +91 9811 747 774 (Mr. Neeraj).
TREMFYA (guselkumab) injection, for subcutaneous use Initial U.S. Approval: 2017
- Summary of Product Characteristics [FDA]: Tremfya (guselkumab) [PDF] Janssen, July 2017
- Janssen Announces US FDA Approval of TREMFYA™ (guselkumab) For The Treatment Of Moderate To Severe Plaque Psoriasis Janssen press release, July 13, 2017
- Tremfya (guselkumab) European Medicines Agency (EMA) information, last checked on Sept 2, 2020
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