DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
GABAPENTIN
FDA Application No:
(ANDA) 075360
Active Ingredient(s):
GABAPENTIN
Company:
APOTEX INC
Label History
Labels are not available on this site for GABAPENTIN, (ANDA) 075360
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/25/2007
005
Labeling
1/29/2003
000
Tentative Approval
Review
4/6/2005
000
Approval
Review
Therapeutic Equivalents
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