DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ALBUTEROL SULFATE
FDA Application No:
(ANDA) 074749
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
HI TECH PHARMA
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 074749
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/21/2001
009
Expiration Date Change
12/21/2001
008
Package Change
12/21/2001
007
Control Supplement
12/21/2001
006
Supplier Addition
2/16/2001
005
Labeling
11/4/1999
004
Chemistry
11/4/1999
003
Labeling
11/4/1999
002
Chemistry
11/4/1999
001
Chemistry
1/30/1998
000
Approval
Therapeutic Equivalents
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