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A generic drug is a copy of the brand-name drug with the same dosage, safety, strength, quality, consumption method, performance, and intended use. Before generics become available on the market, the generic company must prove it has the same active ingredients as the brand-name drug and works in the same way and in the same amount of time in the body.

The only differences between generics and their brand-name counterparts is that generics are less expensive and may look slightly different (eg. different shape or color), as trademarks laws prevent a generic from looking exactly like the brand-name drug.

Generics are less expensive because generic manufacturers don't have to invest large sums of money to develop a drug. When the brand-name patent expires, generic companies can manufacture a copy of the brand-name and sell it at a substantial discount.

Xeomin (IncobotulinumtoxinA)

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Brand

Xeomin (IncobotulinumtoxinA)

Prescription Required

Strength
Qty
50U / Vial
100U / Vial

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  • Product Details

    Description

    Xeomin (incobotulinumtoxinA) is an injectable medication used to treat or improve:

    • Chronic sialorrhea in patients who are least 2 years old
    • Upper limb spasticity in adults
    • Upper limb spasticity (except spasticity caused by cerebral palsy) in pediatric patients who are between 2 and 17 years old
    • Cervical dystonia in adults
    • Blepharospasm in adults
    • The appearance of moderate to severe frown lines between the eyebrows with corrugator and/or procerus muscle activity in adults

    Xeomin may be given intramuscularly or by intraglandular route.

    Fact Table

    Formula

    C6760H10447N1743O2010S32

    License

    US FDA, EMA

    Bioavailability

    Local effect only (no systemic bioavailability)

    Legal status

    Prescription only (Rx)

    Chemical Name

    IncobotulinumtoxinA

    Elimination half-life

    Estimated 18-24 hours

    Dosage (Strength)

    50 units, 100 units per vial (injection)

    Pregnancy

    Consult a doctor

    Brands

    Xeomin

    Protein binding

    N/A (acts locally at neuromuscular junctions)

    PubChem CID

    117048383

    MedlinePlus

    a611011

    ChEBI

    CHEBI:133087

    ATC code

    M03AX01

    DrugBank

    DB00083

    KEGG

    D00959

    Routes of administration

    Intramuscular, intradermal injection

    Directions

    Xeomin may be given intramuscularly or intraglandular by a healthcare professional.

    If you have any questions or concerns, talk to your or your child’s healthcare provider.

    Ingredients

    The active ingredient in Xeomin is incobotulinumtoxinA.

    Inactive ingredients include human albumin and sucrose.

    Contraindications

    Patients who have an infection at the injection sites or who are allergic to botulinum neurotoxin type A or to any of the excipients in Xeomin should not receive it.

    Cautions

    • Xeomin contains the following FDA Boxed Warning:
      • Xeomin’s effects, as well as all botulinum toxin product’s effects, can spread from the injection site to produce symptoms that are consistent with botulinum toxin effects. These symptoms may occur hours to weeks after receiving the injection. Trouble swallowing and breathing can be life threatening; death can also occur. Children treated for spasticity seem to be at greatest risk; however, adults may also experience symptoms, especially those with underlying conditions that would make them more susceptible to these symptoms.
    • Before you or your child begins receiving Xeomin injections, talk to the healthcare provider about:
      • All the prescription and over-the-counter medications you or your child takes
      • Your or your child’s allergies
      • Your or your child’s current health problems and past medical history
      • Your or your child’s pregnancy or breastfeeding status
    • Xeomin contains the following warnings and precautions:
      • Trouble breathing, speaking, or swallowing
      • Corneal exposure and ulceration
      • Risk of ptosis, or drooping of the upper eyelid
      • Xeomin’s potency units are not interchangeable with other botulinum toxin products

    Side Effects

    • Xeomin contains the following FDA Boxed Warning:
      • Xeomin’s effects, as well as all botulinum toxin product’s effects, can spread from the injection site to produce symptoms that are consistent with botulinum toxin effects. These symptoms may occur hours to weeks after receiving the injection. Trouble swallowing and breathing can be life threatening; death can also occur. Children treated for spasticity seem to be at greatest risk; however, adults may also experience symptoms, especially those with underlying conditions that would make them more susceptible to these symptoms.
    • Before you or your child begins receiving Xeomin injections, talk to the healthcare provider about:
      • All the prescription and over-the-counter medications you or your child takes
      • Your or your child’s allergies
      • Your or your child’s current health problems and past medical history
      • Your or your child’s pregnancy or breastfeeding status
    • Xeomin contains the following warnings and precautions:
      • Trouble breathing, speaking, or swallowing
      • Corneal exposure and ulceration
      • Risk of ptosis, or drooping of the upper eyelid
      • Xeomin’s potency units are not interchangeable with other botulinum toxin products

    Side Effects

    The most common Xeomin side effects in patients receiving the injections for treating or improving:

    • Chronic sialorrhea in adults: tooth extraction, dry mouth, diarrhea, and high blood pressure
    • Chronic sialorrhea in pediatric patients: bronchitis, headache, nausea, and vomiting
    • Upper limb spasticity in adults: seizure, nasopharyngitis, dry mouth, and upper respiratory tract infection
    • Upper limb spasticity in pediatric patients: bronchitis and nasopharyngitis
    • Cervical dystonia: trouble swallowing, neck pain, muscle weakness, pain at the injection site, musculoskeletal pain
    • Blepharospasm: eyelid drooping, dry eye, vision problems, and dry mouth
    • Frown lines between the eyebrows: headache

    Immediately notify the health care provider of any side effects that bother you or your child or they persist.

    Ask your or your child’s healthcare provider about Xeomin.

    Reference

    Xeomin. Raleigh, NC and Franksville, WI: Merz Pharmaceuticals, LLC and Merz North America, Inc.; 2023.




    IMPORTANT NOTE: The above information is intended to increase awareness of health information and does not suggest treatment or diagnosis. This information is not a substitute for individual medical attention and should not be construed to indicate that use of the drug is safe, appropriate, or effective for you. See your health care professional for medical advice and treatment.

    Product Code : 11676

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