DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
PREDNISOLONE ACETATE
FDA Application No:
(ANDA) 083398
Active Ingredient(s):
PREDNISOLONE ACETATE
Company:
WATSON LABS
Label History
Labels are not available on this site for PREDNISOLONE ACETATE, (ANDA) 083398
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/19/1999
143
Microbiology
2/2/1999
142
Microbiology
5/27/1998
141
Chemistry
8/6/1997
140
Chemistry
5/9/1991
138
Labeling in Effect
10/26/1989
137
Labeling
1/11/1991
136
Chemistry
1/11/1991
135
Chemistry
12/23/1988
134
Chemistry
12/23/1988
133
Chemistry
12/30/1988
131
SBA
6/16/1986
130
Chemistry
10/31/1984
129
Chemistry
6/27/1984
126
Chemistry
6/27/1984
125
Chemistry
6/27/1984
083
Chemistry
2/13/1974
000
Approval
Therapeutic Equivalents
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