NDC 0019-3183

Conray 43

Iothalamate Meglumine

Conray 43 is a Intravascular Injection in the Human Prescription Drug category. It is labeled and distributed by Liebel-flarsheim Company Llc. The primary component is Iothalamate Meglumine.

Product ID0019-3183_5d4ee8d1-2ed7-427b-81cb-e6fe6f539893
NDC0019-3183
Product TypeHuman Prescription Drug
Proprietary NameConray 43
Generic NameIothalamate Meglumine
Dosage FormInjection
Route of AdministrationINTRAVASCULAR
Marketing Start Date2010-10-11
Marketing CategoryNDA / NDA
Application NumberNDA013295
Labeler NameLiebel-Flarsheim Company LLC
Substance NameIOTHALAMATE MEGLUMINE
Active Ingredient Strength430 mg/mL
Pharm ClassesRadiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0019-3183-15

50 VIAL, GLASS in 1 BOX (0019-3183-15) > 50 mL in 1 VIAL, GLASS
Marketing Start Date2010-10-11
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0019-3183-15 [00019318315]

Conray 43 INJECTION
Marketing CategoryNDA
Application NumberNDA013295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-10-11

NDC 0019-3183-50 [00019318350]

Conray 43 INJECTION
Marketing CategoryNDA
Application NumberNDA013295
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-11
Marketing End Date2019-06-28

NDC 0019-3183-07 [00019318307]

Conray 43 INJECTION
Marketing CategoryNDA
Application NumberNDA013295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-10-11
Marketing End Date2014-09-30

NDC 0019-3183-11 [00019318311]

Conray 43 INJECTION
Marketing CategoryNDA
Application NumberNDA013295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-10-11
Marketing End Date2014-09-30

NDC 0019-3183-09 [00019318309]

Conray 43 INJECTION
Marketing CategoryNDA
Application NumberNDA013295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-10-11

NDC 0019-3183-05 [00019318305]

Conray 43 INJECTION
Marketing CategoryNDA
Application NumberNDA013295
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2010-10-11
Marketing End Date2019-06-28

Drug Details

Active Ingredients

IngredientStrength
IOTHALAMATE MEGLUMINE430 mg/mL

OpenFDA Data

SPL SET ID:77dd7fb3-18c4-4acb-af07-f929dff03903
Manufacturer
UNII
UPC Code
  • 0300193183505
  • Pharmacological Class

    • Radiographic Contrast Agent [EPC]
    • X-Ray Contrast Activity [MoA]

    NDC Crossover Matching brand name "Conray 43" or generic name "Iothalamate Meglumine"

    NDCBrand NameGeneric Name
    0019-3183Conray 43iothalamate meglumine
    0019-0953Conrayiothalamate meglumine
    0019-0862Cysto-Conray IIIothalamate meglumine

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