DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
TAMOXIFEN CITRATE
FDA Application No:
(ANDA) 074539
Active Ingredient(s):
TAMOXIFEN CITRATE
Company:
PHARMACHEMIE
Label History
Labels are not available on this site for TAMOXIFEN CITRATE, (ANDA) 074539
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/31/2003
000
Approval
Letter
Letter
Review
4/3/1997
000
Tentative Approval
Letter
Letter
Review
3/9/1999
000
Tentative Approval
Letter
Letter
Review
3/21/2002
000
Tentative Approval
Letter
Letter
Review
5/31/2000
000
Approval
Letter
Letter
Review
Therapeutic Equivalents
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