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) 076895
Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE
Company:
MORTON GROVE
Label History
Labels are not available on this site for PREDNISOLONE SODIUM PHOSPHATE, (ANDA) 076895
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/4/2004
000
Approval
Therapeutic Equivalents
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