DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ULTRAVIST (PHARMACY BULK)
FDA Application No:
(NDA) 021425
Active Ingredient(s):
IOPROMIDE
Company:
BAYER HLTHC
Original Approval or Tentative Approval Date:
September 20, 2002
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
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
ULTRAVIST (PHARMACY BULK)
IOPROMIDE
62.3%
INJECTABLE; INJECTION
Prescription
Yes
None
ULTRAVIST (PHARMACY BULK)
IOPROMIDE
76.9%
INJECTABLE; INJECTION
Prescription
Yes
None
ULTRAVIST (PHARMACY BULK)
IOPROMIDE
49.9%
INJECTABLE; INJECTION
Prescription
Yes
None
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