DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
METHYLPREDNISOLONE SODIUM SUCCINATE
FDA Application No:
(ANDA) 081267
Active Ingredient(s):
METHYLPREDNISOLONE SODIUM SUCCINATE
Company:
TEVA PARENTERAL
Label History
Labels are not available on this site for METHYLPREDNISOLONE SODIUM SUCCINATE, (ANDA) 081267
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/12/1993
001
Labeling in Effect
11/30/1992
000
Approval
Therapeutic Equivalents
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