DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PEDIAPRED
FDA Application No:
(NDA) 019157
Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE
Company:
UCB INC
Original Approval or Tentative Approval Date:
May 28, 1986
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
PEDIAPRED
PREDNISOLONE SODIUM PHOSPHATE
EQ 5MG BASE/5ML
SOLUTION; ORAL
Prescription
Yes
AA
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