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Stelara hc code

Overview
Stelara Approval History. FDA Approved: Yes (First approved September 25, ) Brand name: Stelara Generic name: ustekinumab Dosage form: Injection Company: Janssen Biotech, Inc. Treatment for: Psoriasis, Psoriatic Arthritis, Crohn's Disease, Maintenance, Ulcerative Colitis Stelara (ustekinumab) is a human interleukin and antagonist indicated for the treatment of moderate to severe. Effective January 1, , the product-specific code for STELARA ® is J, ustekinumab, for intravenous injection, 1 mg. It is important to note that this code represents 1 mg or 1/th of a vial. You should be sure to bill units of J on the claim form for each mg vial of STELARA ® that was used. 2 vials = units. of a code in this policy does not imply that the service described by the code is a covered or non- covered health service. Benefit coverage for health services is . ICD Support ICD Support The ICD Diagnosis Codes for Providers. Please refer to the current policy for the latest codes since these codes are subject to change. The codes provided are not intended to be exhaustive. Please consult your ICD code book for additional information. Jan 17,  · January 17, - Revised: to describe STELARA® (ustekinumab) for Intravenous Administration. Effective January 1, , CMS modified code J to be specific to the administered of STELARA® (ustekinumab) for injection and is NOT appropriate for reimbursement of intravenous administration as this would result in overpayment of the . Stelara ® is intended for use under the guidance and supervision of a physician. Stelara ® should only be administered to patients who will be closely monitored and have regular follow-up visits with a physician. The appropriate dose should be determined by a healthcare provider the patient's current weight at the time of. The NDC Code is assigned to “Stelara ” (also known as: “Ustekinumab”), a human prescription drug labeled by “Janssen Biotech, Inc.”. The product's dosage form is injection, solution, and is administered via form. STELARA ® (ustekinumab) is indicated for the treatment of adult patients with active psoriatic arthritis. STELARA ® can be used alone or in combination with methotrexate (MTX).. STELARA ® (ustekinumab) is indicated for the treatment of patients 12 years or older with moderate to severe plaque psoriasis who are candidates for phototherapy or systemic therapy.

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Stelara - FDA prescribing information, side effects and uses

Effective January 1, , the product-specific code for STELARA ® is J, ustekinumab, for intravenous injection, 1 mg. It is important to note that this code represents 1 mg or 1/th of a vial. You should be sure to bill units of J on the claim form for each mg vial of STELARA ® that was used. 2 vials = units. Jan 17,  · January 17, - Revised: to describe STELARA® (ustekinumab) for Intravenous Administration. Effective January 1, , CMS modified code J to be specific to the administered of STELARA® (ustekinumab) for injection and is NOT appropriate for reimbursement of intravenous administration as this would result in overpayment of the . The NDC Code is assigned to “Stelara ” (also known as: “Ustekinumab”), a human prescription drug labeled by “Janssen Biotech, Inc.”. The product's dosage form is injection, solution, and is administered via form.

 

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