DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
CARTEOLOL HYDROCHLORIDE
FDA Application No:
(ANDA) 075546
Active Ingredient(s):
CARTEOLOL HYDROCHLORIDE
Company:
BAUSCH AND LOMB
Label History
Labels are not available on this site for CARTEOLOL HYDROCHLORIDE, (ANDA) 075546
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/27/2001
008
Microbiology
3/7/2001
007
Microbiology
10/5/2000
006
Microbiology
6/27/2000
005
Microbiology
9/21/2000
004
Control Supplement
8/21/2000
003
Microbiology
5/15/2000
001
Microbiology
1/20/2000
000
Approval
Letter
Therapeutic Equivalents
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