DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
OPTIRAY 240
FDA Application No:
(NDA) 019710
Active Ingredient(s):
IOVERSOL
Company:
MALLINCKRODT
Original Approval or Tentative Approval Date:
December 30, 1988
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
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
OPTIRAY 160
IOVERSOL
34%
INJECTABLE; INJECTION
Prescription
Yes
None
OPTIRAY 240
IOVERSOL
51%
INJECTABLE; INJECTION
Prescription
Yes
None
OPTIRAY 300
IOVERSOL
64%
INJECTABLE; INJECTION
Prescription
Yes
None
OPTIRAY 320
IOVERSOL
68%
INJECTABLE; INJECTION
Prescription
Yes
None
OPTIRAY 350
IOVERSOL
74%
INJECTABLE; INJECTION
Prescription
Yes
None
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