NDC 0407-1414

Omnipaque

Iohexol

Omnipaque is a Intravascular; Intravenous; Oral; Rectal Injection, Solution in the Human Prescription Drug category. It is labeled and distributed by Ge Healthcare Inc.. The primary component is Iohexol.

Product ID0407-1414_064ef67f-cbc0-420d-8bdf-8dbcc5c728bc
NDC0407-1414
Product TypeHuman Prescription Drug
Proprietary NameOmnipaque
Generic NameIohexol
Dosage FormInjection, Solution
Route of AdministrationINTRAVASCULAR; INTRAVENOUS; ORAL; RECTAL
Marketing Start Date2004-09-03
Marketing CategoryNDA / NDA
Application NumberNDA020608
Labeler NameGE Healthcare Inc.
Substance NameIOHEXOL
Active Ingredient Strength350 mg/mL
Pharm ClassesRadiographic Contrast Agent [EPC],X-Ray Contrast Activity [MoA]
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 0407-1414-98

10 BOTTLE, PLASTIC in 1 BOX (0407-1414-98) > 500 mL in 1 BOTTLE, PLASTIC
Marketing Start Date2004-09-03
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 0407-1414-43 [00407141443]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-07-21

NDC 0407-1414-23 [00407141423]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-52 [00407141452]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-45 [00407141445]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-41 [00407141441]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-80 [00407141480]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-31 [00407141431]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26
Marketing End Date2009-11-04

NDC 0407-1414-72 [00407141472]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA020608
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-12-21

NDC 0407-1414-84 [00407141484]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-90 [00407141490]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-26 [00407141426]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26
Marketing End Date2010-10-14

NDC 0407-1414-21 [00407141421]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-85 [00407141485]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-04 [00407141404]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-20 [00407141420]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-93 [00407141493]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-22 [00407141422]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-24 [00407141424]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-36 [00407141436]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26
Marketing End Date2010-10-14

NDC 0407-1414-42 [00407141442]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2006-07-21

NDC 0407-1414-98 [00407141498]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA020608
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2004-09-03

NDC 0407-1414-25 [00407141425]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA020608
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2004-09-03
Marketing End Date2018-11-30

NDC 0407-1414-76 [00407141476]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-94 [00407141494]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-60 [00407141460]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-50 [00407141450]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-89 [00407141489]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-44 [00407141444]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-03 [00407141403]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-87 [00407141487]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-86 [00407141486]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-53 [00407141453]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26

NDC 0407-1414-48 [00407141448]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA020608
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2016-12-21

NDC 0407-1414-51 [00407141451]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

NDC 0407-1414-88 [00407141488]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA020608
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2005-08-03

NDC 0407-1414-37 [00407141437]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1985-12-26
Marketing End Date2010-10-14

NDC 0407-1414-82 [00407141482]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date2006-07-21

NDC 0407-1414-91 [00407141491]

Omnipaque INJECTION, SOLUTION
Marketing CategoryNDA
Application NumberNDA018956
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitML
Marketing Start Date1985-12-26

Drug Details

Active Ingredients

IngredientStrength
IOHEXOL350 mg/mL

OpenFDA Data

SPL SET ID:eee15ebe-d349-4497-acef-6abe7a8247fb
Manufacturer
UNII

Pharmacological Class

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

NDC Crossover Matching brand name "Omnipaque" or generic name "Iohexol"

NDCBrand NameGeneric Name
0407-1401OMNIPAQUEIohexol
0407-1411OMNIPAQUEIohexol
0407-1412OMNIPAQUEIohexol
0407-1413OmnipaqueIohexol
0407-1414OmnipaqueIohexol
0407-1415OMNIPAQUEOMNIPAQUE
0407-1416OMNIPAQUEOMNIPAQUE

Trademark Results [Omnipaque]

Mark Image

Registration | Serial
Company
Trademark
Application Date
OMNIPAQUE
OMNIPAQUE
73340246 1207823 Live/Registered
Sterling Drug Inc.
1981-12-07

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.