DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DELFEN
FDA Application No:
(NDA) 014349
Active Ingredient(s):
NONOXYNOL-9
Company:
PERSONAL PRODS
Label History
Labels are not available on this site for DELFEN, (NDA) 014349
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
3/27/1989
033
Manufacturing Change or Addition
7/29/1988
032
Manufacturing Change or Addition
3/31/1988
031
Control Supplement
3/18/1986
030
Expiration Date Change
9/18/1984
029
Control Supplement
5/14/1980
026
Control Supplement
4/23/1980
025
Distributor
10/27/1980
024
Package Change
3/6/1980
023
Expiration Date Change
3/24/1980
022
Manufacturing Change or Addition
7/31/1979
021
Package Change
7/31/1979
020
Package Change
7/31/1979
019
Package Change
2/23/1978
014
Package Change
4/17/1978
012
Control Supplement
12/10/1963
000
Approval
There are no Therapeutic Equivalents
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