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) 076123
Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE
Company:
PHARM ASSOC
Label History
Labels are not available on this site for PREDNISOLONE SODIUM PHOSPHATE, (ANDA) 076123
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/23/2002
000
Approval
5/13/2002
000
Tentative Approval
Therapeutic Equivalents
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