DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
THIAMINE HYDROCHLORIDE
FDA Application No:
(ANDA) 080556
Active Ingredient(s):
THIAMINE HYDROCHLORIDE
Company:
ABRAXIS PHARM
Label History
Labels are not available on this site for THIAMINE HYDROCHLORIDE, (ANDA) 080556
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/30/1998
023
Chemistry
11/7/1997
022
Chemistry
11/4/1994
021
Chemistry in Effect
11/4/1994
020
Chemistry in Effect
8/30/1996
019
Chemistry
12/4/1990
018
Labeling
9/29/1983
016
Chemistry
6/20/1972
000
Approval
Therapeutic Equivalents
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