DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
KETAMINE HYDROCHLORIDE
FDA Application No:
(ANDA) 076092
Active Ingredient(s):
KETAMINE HYDROCHLORIDE
Company:
BIONICHE PHARMA
Label History
Labels are not available on this site for KETAMINE HYDROCHLORIDE, (ANDA) 076092
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/25/2002
002
Labeling
10/25/2002
001
Chemistry New Strength
12/28/2001
000
Approval
Letter
Review
Therapeutic Equivalents
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