DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PANTOPRAZOLE SODIUM
FDA Application No:
(ANDA) 077058
Active Ingredient(s):
PANTOPRAZOLE SODIUM
Company:
SUN PHARM INDS
Label History
Labels are not available on this site for PANTOPRAZOLE SODIUM, (ANDA) 077058
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/22/2006
000
Tentative Approval
9/10/2007
000
Approval
Therapeutic Equivalents
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