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) 074524
Active Ingredient(s):
KETAMINE HYDROCHLORIDE
Company:
BEDFORD
Label History
Labels are not available on this site for KETAMINE HYDROCHLORIDE, (ANDA) 074524
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/3/2001
003
Microbiology
9/24/1999
001
Labeling
3/22/1996
000
Approval
Therapeutic Equivalents
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