WebThe NDC code 47335-177 is assigned by the FDA to the product Ilumya which is a human prescription drug product labeled by Sun Pharmaceutical Industries, Inc.. The generic name of Ilumya is tildrakizumab-asmn. The product's dosage form is injection, solution and is administered via subcutaneous form. The product is distributed in 4 packages with ... WebThe NDC Packaged Code 47335-177-95 is assigned to a package of 1 ml in 1 carton of Ilumya, a human prescription drug labeled by Sun Pharmaceutical Industries, Inc.. The product's dosage form is injection, solution and is administered via subcutaneous form.This product is billed per "ML" milliliter and contains an estimated amount of 1 billable ...
ILUMYA® (tildrakizumab-asmn) - YouTube
WebLearn about Ilumya (tildrakizumab), potential side effects, proper use and dosing, and popular alternatives. Read reviews from GoodRx ... and then every 3 months thereafter. … WebILUMYA is a drug for treatment of moderate to severe plaque psoriasis, in adults, who may benefit from taking injections or pills (systemic therapy) or treatment using ultraviolet or … f x 4x 2 3x 13 find f 1
Tildrakizumab - Wikipedia
Web3 apr. 2024 · ILUMYA™ is indicated for the treatment of adults with moderate-to-severe plaque psoriasis who are candidates for systemic therapy or phototherapy. 2.1 Dosage. ILUMYA is administered by subcutaneous injection. The recommended dose is 100 mg at Weeks 0, 4, and every twelve weeks thereafter. Each syringe contains 1 mL of 100 … Web22 feb. 2024 · Both brand names start with the letters “I-L,” and both products are used for inflammatory conditions, are injectable drugs administered subcutaneously, and are … WebILUMYA (tildrakizumab-asmn) is an injectable solution that contains an interleukin-23 (IL-23) antagoinst. ILUMYA is administered as subcutaneous injection of 100mg at week 0, … glasfaser switch 24 port