DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
OMNIPAQUE 210
FDA Application No:
(NDA) 018956
Active Ingredient(s):
IOHEXOL
Company:
GE HEALTHCARE
Original Approval or Tentative Approval Date:
December 26, 1985
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
OMNIPAQUE 140
IOHEXOL
30.2%
INJECTABLE; INJECTION
Prescription
Yes
None
OMNIPAQUE 180
IOHEXOL
38.8%
SOLUTION; INJECTION, ORAL, RECTAL
Prescription
Yes
None
OMNIPAQUE 210
IOHEXOL
45.3%
INJECTABLE; INJECTION
Discontinued
No
None
OMNIPAQUE 240
IOHEXOL
51.8%
SOLUTION; INJECTION, ORAL, RECTAL
Prescription
Yes
None
OMNIPAQUE 300
IOHEXOL
64.7%
SOLUTION; INJECTION, ORAL, RECTAL
Prescription
Yes
None
OMNIPAQUE 350
IOHEXOL
75.5%
SOLUTION; INJECTION, ORAL
Prescription
Yes
None
OMNIPAQUE 70
IOHEXOL
15.1%
SOLUTION; URETHRAL
Discontinued
No
None
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