Visitor Monitoring Drug History: ERYTHROCIN
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
Browse by Letter: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 0-9
Label and Approval History

Drug Name: ERYTHROCIN
FDA Application No: (NDA) 050182
Active Ingredient(s): ERYTHROMYCIN LACTOBIONATE
Company: HOSPIRA
 
Label History
 
Labels are not available on this site for ERYTHROCIN, (NDA) 050182
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
9/16/2004 125Labeling Revision Letter 
12/13/2002 124Expiration Date Change  
8/29/2002 123Control Supplement  
5/23/2002 122Labeling Revision Letter 
4/23/1999 121Control Supplement  
10/27/1997 119Package Change  
3/18/1996 118Package Change  
10/6/1983 117Formulation Revision  
9/23/1982 116Control Supplement  
5/21/1982 115Control Supplement  
4/6/1982 114Control Supplement  
11/10/1981 113Package Change  
10/7/1981 112Labeling Revision  
9/16/1981 111Control Supplement  
6/5/1981 110Control Supplement  
5/20/1981 109Package Change  
5/14/1981 108Control Supplement  
4/28/1981 107Control Supplement  
3/3/1981 106Control Supplement  
1/30/1981 105Labeling Revision  
12/17/1980 104Labeling Revision  
10/21/1980 102Labeling Revision  
10/21/1980 101Labeling Revision  
9/23/1980 100Control Supplement  
9/4/1980 099Control Supplement  
8/19/1980 098Labeling Revision  
7/23/1980 097Labeling Revision  
7/17/1980 096Labeling Revision  
7/15/1980 095Labeling Revision  
6/26/1980 094Labeling Revision  
5/23/1980 093Labeling Revision  
5/21/1980 092Control Supplement  
5/22/1980 091Control Supplement  
5/7/1980 090Control Supplement  
5/6/1980 089Labeling Revision  
5/6/1980 088Labeling Revision  
5/7/1980 087Formulation Revision  
4/25/1980 086Control Supplement  
3/26/1980 085Control Supplement  
3/25/1980 084Labeling Revision  
3/25/1980 083Control Supplement  
3/17/1980 082Labeling Revision  
3/12/1980 081Control Supplement  
2/15/1980 080Formulation Revision  
1/14/1980 079Labeling Revision  
1/4/1980 078Formulation Revision  
1/16/1980 077Expiration Date Change  
12/17/1979 076Control Supplement  
11/23/1979 075Formulation Revision  
11/6/1979 074Labeling Revision  
11/6/1979 073Labeling Revision  
9/18/1979 072Control Supplement  
8/27/1979 071Formulation Revision  
8/22/1979 070Control Supplement  
10/10/1979 069Control Supplement  
6/20/1979 068Control Supplement  
6/19/1979 067Control Supplement  
5/21/1979 066Control Supplement  
5/4/1979 065Control Supplement  
7/19/1979 064Package Change  
4/13/1979 063Control Supplement  
3/29/1979 062Control Supplement  
4/5/1979 061Package Change  
3/20/1979 060Labeling Revision  
3/29/1979 059Package Change  
3/7/1979 058Control Supplement  
3/9/1979 057Control Supplement  
1/19/1979 056Labeling Revision  
1/8/1979 055Control Supplement  
12/13/1978 054Control Supplement  
12/7/1978 053Control Supplement  
12/4/1978 052Formulation Revision  
10/30/1978 050Control Supplement  
9/25/1978 049Labeling Revision  
6/7/1978 048Formulation Revision  
5/25/1978 047Control Supplement  
8/9/1977 046Formulation Revision  
6/10/1977 045Control Supplement  
1/7/1975 043Labeling Revision  
5/17/1972 042Labeling Revision  
5/10/1974 041New or Modified Indication  
11/19/1971 040Labeling Revision  
4/27/1971 039Labeling Revision  
9/19/1968 038Labeling Revision  
6/15/1967 037Labeling Revision  
4/18/1967 036Labeling Revision  
12/30/1966 035Formulation Revision  
12/16/1966 034Labeling Revision  
5/31/1966 033Labeling Revision  
1/14/1966 032Labeling Revision  
10/8/1965 031Manufacturing Change or Addition  
9/15/1965 030Labeling Revision  
10/5/1965 029Control Supplement  
3/12/1993 028Labeling Revision  
10/11/1996 027Labeling Revision  
12/5/1991 026Chemistry Generic  
5/3/1991 023Labeling Revision  
11/30/1988 022Control Supplement  
12/30/1987 021Labeling Revision  
5/11/1965 020Labeling Revision  
5/4/1965 019Labeling Revision  
2/10/1965 018Labeling Revision  
10/27/1964 016Labeling Revision  
10/26/1964 015Labeling Revision  
5/16/1984 014Control Supplement  
9/25/1984 013Control Supplement  
12/20/1983 012Formulation Revision  
11/9/1983 011Labeling Revision  
11/1/1983 010Labeling Revision  
7/22/1983 009Manufacturing Change or Addition  
6/2/1983 008Control Supplement  
5/27/1983 007Control Supplement  
9/22/1964 006Labeling Revision  
8/20/1964 005Labeling Revision  
8/5/1964 004Labeling Revision  
7/17/1964 003Labeling Revision  
10/8/1982 002Control Supplement  
7/13/1964 001Labeling Revision  
6/25/1964 000Approval  
 
Therapeutic Equivalents
©2019 Drugs That Causes a False Positive on a Drug Test