DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CARBIDOPA AND LEVODOPA
FDA Application No:
(ANDA) 077828
Active Ingredient(s):
CARBIDOPA; LEVODOPA
Company:
SUN PHARM INDS
Label History
Labels are not available on this site for CARBIDOPA AND LEVODOPA, (ANDA) 077828
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/23/2007
000
Approval
There are no Therapeutic Equivalents
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