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) 075099
Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE
Company:
MORTON GROVE
Label History
Labels are not available on this site for PREDNISOLONE SODIUM PHOSPHATE, (ANDA) 075099
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/28/2002
000
Approval
Letter
Therapeutic Equivalents
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