DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METHYLPREDNISOLONE
FDA Application No:
(ANDA) 087535
Active Ingredient(s):
METHYLPREDNISOLONE SODIUM SUCCINATE
Company:
ORGANON USA INC
Label History
Labels are not available on this site for METHYLPREDNISOLONE, (ANDA) 087535
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/12/1985
005
Chemistry
4/12/1985
003
Chemistry
2/28/1983
001
Chemistry
6/25/1982
000
Approval
Therapeutic Equivalents
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