DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NAPROXEN
FDA Application No:
(ANDA) 077339
Active Ingredient(s):
NAPROXEN
Company:
PERRIGO R AND D
Label History
Labels are not available on this site for NAPROXEN, (ANDA) 077339
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/27/2005
000
Approval
Therapeutic Equivalents
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