DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HYPAQUE
FDA Application No:
(NDA) 009561
Active Ingredient(s):
DIATRIZOATE SODIUM
Company:
GE HEALTHCARE
Original Approval or Tentative Approval Date:
November 26, 1954
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority 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
HYPAQUE
DIATRIZOATE SODIUM
50%
INJECTABLE; INJECTION
Prescription
Yes
None
HYPAQUE
DIATRIZOATE SODIUM
25%
INJECTABLE; INJECTION
Discontinued
No
None
HYPAQUE SODIUM 20%
DIATRIZOATE SODIUM
20%
SOLUTION; URETERAL
Discontinued
No
None
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