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) 072630
Active Ingredient(s):
ALBUTEROL SULFATE
Company:
WATSON LABS
Label History
Labels are not available on this site for ALBUTEROL SULFATE, (ANDA) 072630
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
2/1/1993
002
Labeling in Effect
10/21/1991
001
Chemistry
1/31/1991
000
Approval
Therapeutic Equivalents
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