DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SECONAL SODIUM
FDA Application No:
(NDA) 007392
Active Ingredient(s):
SECOBARBITAL SODIUM
Company:
LILLY
Label History
Labels are not available on this site for SECONAL SODIUM, (NDA) 007392
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/5/1982
006
Labeling Revision
6/24/1981
005
Manufacturing Change or Addition
7/23/1974
003
Supplement Amendment (MarkIV)
7/19/1950
000
Approval
Other Important Information from FDA
Therapeutic Equivalents
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