Visitor Monitoring Drug History: OPTICROM
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: OPTICROM
FDA Application No: (NDA) 018155
Active Ingredient(s): CROMOLYN SODIUM
Company: ALLERGAN
 
Label History
 
Labels are not available on this site for OPTICROM, (NDA) 018155
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
4/12/2002 026Control Supplement  
12/4/2001 025Manufacturing Change or Addition  
4/12/2001 024Manufacturing Change or Addition  
7/24/2001 023Manufacturing Change or Addition  
2/13/2001 022Labeling Revision  
10/2/2000 021Manufacturing Change or Addition  
3/3/1998 020Manufacturing Change or Addition  
6/11/1993 018New Dosage Regimen  
7/22/1992 017Package Change  
10/13/1992 016Manufacturing Change or Addition  
2/9/1990 013Manufacturing Change or Addition  
4/4/1989 012Package Change  
9/23/1987 011Control Supplement  
4/23/1987 010Expiration Date Change  
10/24/1986 008Manufacturing Change or Addition  
3/12/1987 007Package Change  
12/2/1986 006Package Change  
6/20/1986 005Package Change  
6/28/1985 004Package Change  
12/23/1985 003Manufacturing Change or Addition  
7/24/1985 002Control Supplement  
1/16/1985 001Control Supplement  
10/3/1984 000Approval  
 
Therapeutic Equivalents
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