DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ALBALON
FDA Application No:
(ANDA) 080248
Active Ingredient(s):
NAPHAZOLINE HYDROCHLORIDE
Company:
ALLERGAN
Label History
Labels are not available on this site for ALBALON, (ANDA) 080248
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/15/2002
042
Microbiology
7/3/2002
040
Microbiology
11/15/2001
039
Facility Addition
8/15/2001
038
Facility Addition
12/8/2000
037
Facility Addition
8/24/1998
036
Chemistry
3/18/1999
035
Microbiology
9/29/1997
034
Chemistry
9/29/1997
033
Chemistry
6/21/1995
032
Chemistry
6/21/1995
031
Chemistry
9/27/1994
030
Chemistry
5/7/1992
029
Chemistry
3/25/1991
028
Labeling
1/20/1988
026
Chemistry
6/5/1987
025
Chemistry
5/12/1983
020
Chemistry
3/24/1972
000
Approval
Therapeutic Equivalents
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