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) 075183
Active Ingredient(s):
PREDNISOLONE SODIUM PHOSPHATE
Company:
HI TECH PHARMA
Label History
Labels are not available on this site for PREDNISOLONE SODIUM PHOSPHATE, (ANDA) 075183
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/17/2002
000
Tentative Approval
3/26/2003
000
Approval
Therapeutic Equivalents
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