DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
BENZEDRINE
FDA Application No:
(ANDA) 083900
Active Ingredient(s):
AMPHETAMINE SULFATE
Company:
SMITH KLINE & FRENCH
Label History
Labels are not available on this site for BENZEDRINE, (ANDA) 083900
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/11/1981
009
Supplement
Review
12/14/1979
008
Supplement
Review
5/11/1982
007
Chemistry
Review
2/6/1979
006
Supplement
Review
2/11/1981
005
Supplement
Review
11/21/1978
004
Supplement
Review
11/21/1978
003
Supplement
Review
5/11/1977
002
Supplement
Review
4/15/1976
001
Supplement
Review
2/26/1976
000
Approval
Review
Therapeutic Equivalents
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