DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ENDOSOL EXTRA
FDA Application No:
(NDA) 020079
Active Ingredient(s):
CALCIUM CHLORIDE; DEXTROSE; GLUTATHIONE DISULFIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; SODIUM CHLORIDE; SODIUM PHOSPHATE
Company:
AKORN
Label History
Labels are not available on this site for ENDOSOL EXTRA, (NDA) 020079
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/16/1996
003
Labeling
4/16/1996
002
Labeling
5/12/1992
001
Labeling
11/27/1991
000
Approval
There are no Therapeutic Equivalents
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