DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
CEDAX
FDA Application No:
(NDA) 050686
Active Ingredient(s):
CEFTIBUTEN DIHYDRATE
Company:
SHIONOGI
Original Approval or Tentative Approval Date:
December 20, 1995
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
CEDAX
CEFTIBUTEN DIHYDRATE
EQ 90MG BASE/5ML
FOR SUSPENSION; ORAL
Prescription
Yes
None
CEDAX
CEFTIBUTEN DIHYDRATE
EQ 180MG BASE/5ML
FOR SUSPENSION; ORAL
Discontinued
No
None
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