DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PREDNISOLONE SODIUM PHOSPHATE
FDA Application No:
(ANDA) 076913
Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE
Company:
PHARM ASSOC
Label History
Labels are not available on this site for PREDNISOLONE SODIUM PHOSPHATE, (ANDA) 076913
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/5/2007
002
Control Supplement
4/25/2005
000
Approval
Therapeutic Equivalents
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