DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
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
Original Approval or Tentative Approval Date:
June 16, 2003
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Label Information
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
INFUVITE ADULT
ALPHA-TOCOPHEROL ACETATE; ASCORBIC ACID; BIOTIN; CHOLECALCIFEROL; CYANOCOBALAMIN; DEXPANTHENOL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A PALMITATE; VITAMIN K
2 IU/ML; 40MG/ML; 12UGM/ML; 40 IU/ML; 1UGM/ML; 3MG/ML; 120UGM/ML; 8MG/ML; 1.2MG/ML; 0.72MG/ML; 1.2MG/ML; 660 IU/ML; 30UGM/ML
INJECTABLE; IV (INFUSION)
Prescription
Yes
None
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