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Iothalamate Meglumine (Cysto-Conray Ii)

Trade Name : Cysto-Conray II

Liebel-Flarsheim Company LLC

INJECTION

Strength 172 mg/mL

IOTHALAMATE MEGLUMINE Radiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]

Delivery Process

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Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Iothalamate Meglumine (Cysto-Conray Ii) which is also known as Cysto-Conray II and Manufactured by Liebel-Flarsheim Company LLC. It is available in strength of 172 mg/mL per ml. Read more

Iothalamate Meglumine (Cysto-Conray Ii) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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  • No data
  • NOT FOR INTRAVASCULAR ADMINISTRATION
  • NOT FOR INTRATHECAL USE
  • Cysto-Conray II is a sterile aqueous solution intended for instillation as a diagnostic radiopaque medium. Cysto-Conray II contains 17.2% w/v iothalamate meglumine which is 1-Deoxy-1-(methylamino)-D-glucitol 5-acetamido-2,4,6-triiodo-N-methylisophthalamate (salt) and has the following structural formula:
  • Each milliliter of Cysto-Conray II contains 172 mg of iothalamate meglumine, equivalent to 81 mg (8.1% w/v) of organically bound iodine, 0.110 mg edetate calcium disodium as a stabilizer and 0.115 mg of monobasic sodium phosphate as a buffer.
  • Cysto-Conray II is hypertonic under conditions of use and is supplied in containers from which the air has been displaced by nitrogen. The pH of Cysto-Conray II is 6.6 to 7.6.
  • The most important characteristic of contrast media is the iodine content.u00a0 The relatively high atomic weight of iodine contributes sufficient radiodensity for radiographic contrast.
  • Following instillation by sterile catheter, Cysto-Conray II provides for visualization of the lower urinary tract. Clinical literature reports indicate that routinely less thanu00a01 percent of a retrograde urographic radiopaque is absorbed systemically, however, as much as 12 percent absorption was observed with pyelorenal back flow and may produce iodine medicated thyrotropic effects described under .
  • Cysto-Conray II is indicated for use in retrograde cystography and cystourethrography.
  • See concerning inadvertant intrathecal administration.
  • SEVERE ADVERSE EVENTS u2013 INADVERTENT INTRATHECAL ADMINISTRATION:
  • No data
  • Irritation of the bladder or ureter, common to some degree to all contrast media administered for retrograde urographic procedures, may occasionally occur.
  • As with all contrast media, intravasation may lead to hypersensitivity reactions such as a sense of warmth, flushing, sneezing, sweating, chills, fever, urticaria, laryngeal edema, bronchospasm, hypertension, hypotension, cardiac arrhythmias and cardiac arrest.
  • Adverse reactions associated with procedural technique include injury to the urethra, bladder, ureter, and introduction of infection.
  • In the event of serious or anaphylactoid reactions, it should be kept in mind that the reactions known to occur with intravenous administration of radiopaque contrast materials are possible.
  • No data
  • Store at 20u00b0 to 25u00b0C (68u00b0 to 77u00b0F) [see USP Controlled Room Temperature]. Exposing this product to very cold temperatures may result in crystallization of the salt. If this occurs, the containers should be brought to room temperature. Shake vigorously to assure complete dissolution of any crystals. The speed of dissolution may be increased by heating with circulating warm air. Before use, examine the product to assure that all solids are redissolved and that the container and closure have not been damaged.
  • This product is sensitive to light and must be protected from strong daylight or direct exposure to the sun.
  • As with all contrast media, the containers should be inspected prior to use to ensure that breakage or other damage has not occurred during shipping and handling. All containers should be inspected for closure integrity. Damaged containers should not be used.
  • Manufactured by: Liebel-Flarsheim Company LLCRaleigh, NC 27616u00a0
  • Made in USA
  • GBT 0862A0817Revised 08/17u00a0u00a0u00a0u00a0u00a0
  • Guerbet
  • Not For Intravascular AdministrationSterile Solution
  • Cysto-Conray lln- 250 mL
  • Iothalamate Meglumine Injection USP 17.2%
  • NOT FOR INTRATHECAL USERx Only
  • Protect from light u2022n- Single dose container u2022 Discard unused portionUsual Dosage:
  • 10230419
  • Guerbet
  • Manufactured by:Liebel-Flarsheim Company LLCRaleigh, NC 27616
  • Made in USA

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