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HomeShopGnRG AntagonistCETRORELIX ACETATE INJECTION
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CETRORELIX ACETATE INJECTION
Categories:GnRG Antagonist, Hormonal Therapy Product SKU: 00001-3
CETRORELIX ACETATE INJECTION

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Description

PRODUCT DESCRIPTION:

Cetrorelix Acetate is a synthetic gonadotropin-releasing hormone (GnRH) antagonist used to prevent premature luteinizing hormone (LH) surges in women undergoing controlled ovarian stimulation for assisted reproductive technologies (ART), including IVF.

Unlike GnRH agonists, Cetrorelix provides immediate suppression of LH without an initial hormonal flare, allowing for better cycle control and reduced risk of ovarian hyperstimulation syndrome (OHSS).

Formulation & Presentation:

  • Dosage Form: Lyophilized Powder for Reconstitution
  • Presentation: Sterile Vial/ Pre-Filled Syringes (PFS) Also Available
  • Available Strengths: 0.25 MG Injection

Route of Administration:

  • Subcutaneous (As per indication & Specialist Directions)

Therapeutic Indications:

  • Prevention of premature LH surges in women undergoing controlled ovarian stimulation for ART
  • IVF and embryo transfer cycle management

Side Effects:

  • COMMON: Mild abdominal pain, injection site redness or itching, headache, nausea, fatigue.
  • SERIOUS (RARE): Ovarian hyperstimulation syndrome (OHSS), hypersensitivity reactions, shortness of breath, hives.
  • PRECAUTIONS: Should be administered under expert medical supervision.
    • Monitoring of ovarian response and hormone levels is critical.
    • Use with caution in patients with known hypersensitivity to GnRH analogues

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TECHNICAL INFORMATION

Product Specifications:

  • HSN Code: 300439
  • Weight: Approx. 40g per vial (With Packaging)
  • Dimensions: 8 cm × 3 cm × 3 cm
  • Shelf Life (Subject To Country Specific Guidelines): 24 months from date of manufacture
  • Storage: Store strictly between 2°C to 8°C. Protect from light. Do not freeze.

Regulatory Status & Supply Information:

  • Regulatory Status: USFDA/WHO-GMP Complaint Manufacturing. Further certifications available on request
  • Exports Ready Dossiers: Dossier Available (CTD/eCTD formats)
  • Stability: Zone IVB Compliant
  • MOQ: Negotiable. Based on market & registration status

Who Should Source This Product?

  • Fertility clinics and ART centers
  • National ART Programs or reproductive health programs
  • Distributors of hormone-based injectables or Women’s reproductive Health programs
  • NGOs and procurement agencies in reproductive care focusing in infertility treatment

Why Source from PHARMET?

  • Single-window sourcing for diverse pharma needs
  • Export-ready documentation & regulatory support
  • Adaptable documentation support for effective registration support in
  • Trusted consortium network, simplifying India’s complex pharma supply chain
  • Multiple approved manufacturers for best fit in import country
  • Network of audited, compliant manufacturers across India
  • Customizable & Flexible branding, packaging & formulation flexibility
  • End to End Logistics support flexibility & support.
  • Deep expertise in exporting specialty injectables & ART products

CONTACT DETAILS:

  • E-MAIL: connect@pharmet.io
  • Phone/WhatsApp Number: +91 9999091881
  • Website: www.pharmet.io

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