DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PREDNISOLONE
FDA Application No:
(ANDA) 080342
Active Ingredient(s):
PREDNISOLONE
Company:
WHITEWORTH TOWN PLSN
Label History
Labels are not available on this site for PREDNISOLONE, (ANDA) 080342
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/26/1985
006
Chemistry
11/26/1985
005
Chemistry
Therapeutic Equivalents
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