DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
FDA Application No:
(ANDA) 078177
Active Ingredient(s):
SODIUM CHLORIDE
Company:
FRESENIUS MEDCL
Label History
Labels are not available on this site for SODIUM CHLORIDE 0.9 IN PLASTIC CONTAINER, (ANDA) 078177
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
4/12/2007
000
Approval
Therapeutic Equivalents
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