CONRAY Solution for injection Ref.[10334] Active ingredients: Iotalamic acid

Source: FDA, National Drug Code (US)  Revision Year: 2019 

Product description

Conray is a sterile aqueous solution intended for use as a diagnostic radiopaque medium. Conray contains 60% 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 contains 600 mg of iothalamate meglumine, 0.09 mg edetate calcium disodium as a stabilizer and 0.125 mg of monobasic sodium phosphate as a buffer. The solution provides 28.2% (282 mg/mL) organically bound iodine. Conray has an osmolarity of approximately 1000 mOsmol per liter, an osmolality of approximately 1400 mOsmol per kilogram and is, therefore, hypertonic under conditions of use. The viscosity (cps) is approximately 6 at 25°C and 4 at 37°C. The pH is 6.5 to 7.7.

Conray is a clear solution containing no undissolved solids. Crystallization does not occur at normal room temperatures. It is supplied in containers from which the air has been displaced by nitrogen.

How Supplied
Conray Glass Vials/Bottles NDC Number
25x30 mL vials 0019-0953-23
25x50 mL vials 0019-0953-05
12x100 mL bottles 0019-0953-10
12x150 mL bottles 0019-0953-50

Manufactured by: Liebel-Flarsheim Company LLC, Raleigh, NC 27616, Made in USA

Drugs

Drug Countries
CONRAY Canada, United States, South Africa

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