DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BETADERM
FDA Application No:
(NDA) 018839
Active Ingredient(s):
BETAMETHASONE VALERATE
Company:
ROACO
Label History
Labels are not available on this site for BETADERM, (NDA) 018839
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
6/30/1983
000
Approval
Therapeutic Equivalents
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