DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
HEPARIN SODIUM
FDA Application No:
(NDA) 005521
Active Ingredient(s):
HEPARIN SODIUM
Company:
LILLY
Label History
Labels are not available on this site for HEPARIN SODIUM, (NDA) 005521
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
5/23/2000
026
Manufacturing Change or Addition
6/5/1998
024
Control Supplement
1/31/1996
023
Manufacturing Change or Addition
11/29/1989
021
Labeling Revision
10/27/1989
020
Labeling Revision
4/27/1999
019
Expiration Date Change
6/1/1989
018
Labeling Revision
6/1/1989
017
Labeling Revision
5/13/1985
016
Practioner Draft Labeling
6/16/1981
015
Manufacturing Change or Addition
3/19/1981
014
Control Supplement
9/7/1979
013
Control Supplement
1/17/1980
012
Labeling Revision
7/8/1982
011
Control Supplement
3/18/1976
008
Control Supplement
5/19/1944
000
Approval
Therapeutic Equivalents
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