DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CYCLOBENZAPRINE HYDROCHLORIDE
FDA Application No:
(ANDA) 072854
Active Ingredient(s):
CYCLOBENZAPRINE HYDROCHLORIDE
Company:
SANDOZ
Label History
Labels are not available on this site for CYCLOBENZAPRINE HYDROCHLORIDE, (ANDA) 072854
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/3/2006
015
Chemistry New Strength
2/3/2006
014
Chemistry New Strength
8/27/2001
009
Control Supplement
1/21/2000
008
Control Supplement
5/5/1999
007
Chemistry
2/5/1999
006
Chemistry
2/5/1999
005
Labeling
2/5/1999
004
Chemistry
9/26/1997
003
Chemistry
4/22/1994
002
Labeling
1/24/1994
001
Chemistry
11/19/1991
000
Approval
Therapeutic Equivalents
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