NDC 0019-1324

Optiray 240

Ioversol

Optiray 240 is a Intra-arterial; Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Liebel-flarsheim Company Llc. The primary component is Ioversol.

Product ID0019-1324_0d687753-5c3f-47b3-921e-4c2f22ba6717
NDC0019-1324
Product TypeHuman Prescription Drug
Proprietary NameOptiray 240
Generic NameIoversol
Dosage FormInjection
Route of AdministrationINTRA-ARTERIAL; INTRAVENOUS
Marketing Start Date2012-03-04
Marketing CategoryNDA / NDA
Application NumberNDA019710
Labeler NameLiebel-Flarsheim Company LLC
Substance NameIOVERSOL
Active Ingredient Strength509 mg/mL
Pharm ClassesRadiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0019-1324-06

25 BOTTLE, GLASS in 1 CARTON (0019-1324-06) > 50 mL in 1 BOTTLE, GLASS
Marketing Start Date2012-03-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0019-1324-06 [00019132406]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04

NDC 0019-1324-21 [00019132421]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04

NDC 0019-1324-16 [00019132416]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04
Marketing End Date2016-03-07

NDC 0019-1324-81 [00019132481]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04

NDC 0019-1324-11 [00019132411]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04

NDC 0019-1324-78 [00019132478]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04

NDC 0019-1324-87 [00019132487]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04

NDC 0019-1324-27 [00019132427]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2012-03-04

NDC 0019-1324-75 [00019132475]

Optiray 240 INJECTION
Marketing CategoryNDA
Application NumberNDA019710
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2012-03-04

Drug Details

Active Ingredients

IngredientStrength
IOVERSOL509 mg/mL

OpenFDA Data

SPL SET ID:549d38db-d4ed-4708-8f76-7cdaa157063f
Manufacturer
UNII
UPC Code
  • 0300191323873
  • 0300191324870
  • 0300191332905
  • 0300191333872
  • Pharmacological Class

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

    NDC Crossover Matching brand name "Optiray 240" or generic name "Ioversol"

    NDCBrand NameGeneric Name
    0019-1323OptirayIoversol
    0019-1324OptirayIoversol
    0019-1332OptirayIoversol
    0019-1333OptirayIoversol

    Trademark Results [Optiray]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    OPTIRAY
    OPTIRAY
    73710159 1526467 Live/Registered
    MALLINCKRODT, INC.
    1988-02-08

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