Visitor Monitoring Drug History: INFUVITE ADULT
 
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: INFUVITE ADULT
FDA Application No: (NDA) 021559
Active Ingredient(s): ALPHA-TOCOPHEROL ACETATE; ASCORBIC ACID; BIOTIN; CHOLECALCIFEROL; CYANOCOBALAMIN; DEXPANTHENOL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A PALMITATE; VITAMIN K
Company: SANDOZ
 
Label History
 
View the label approved on June 22, 2003 for INFUVITE ADULT, (NDA) 021559


To see older, previously-approved labels, go to the "Approval History" section of this page. Older labels are for historical information only and should not be used for clinical purposes.
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/13/2004 005Control Supplement Letter 
6/16/2003 000Approval Letter
Label
Review 
 
There are no Therapeutic Equivalents
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