DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
RUBRAMIN PC
FDA Application No:
(NDA) 006799
Active Ingredient(s):
CYANOCOBALAMIN
Company:
BRISTOL MYERS SQUIBB
Label History
Labels are not available on this site for RUBRAMIN PC, (NDA) 006799
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
11/28/1995
015
Labeling Revision
10/14/1987
013
Control Supplement
5/5/1986
012
Control Supplement
10/1/1984
011
Labeling Revision
7/9/1984
010
Labeling Revision
7/31/1985
009
Manufacturing Change or Addition
12/15/1983
008
Labeling Revision
8/26/1980
007
Labeling Revision
1/19/1979
006
Labeling Revision
9/29/1950
000
Approval
Therapeutic Equivalents
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