DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TAZTIA XT
FDA Application No:
(ANDA) 075401
Active Ingredient(s):
DILTIAZEM HYDROCHLORIDE
Company:
ANDRX PHARMS
Label History
Labels are not available on this site for TAZTIA XT, (ANDA) 075401
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/29/2000
000
Tentative Approval
Letter
Review
5/14/2001
000
Tentative Approval
Letter
Review
4/10/2003
000
Approval
Letter
Review
Therapeutic Equivalents
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