DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER
FDA Application No:
(NDA) 020488
Active Ingredient(s):
MAGNESIUM SULFATE
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
July 11, 1995
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER
MAGNESIUM SULFATE
1GM/100ML
INJECTABLE; INJECTION
Prescription
Yes
None
MAGNESIUM SULFATE IN DEXTROSE 5% IN PLASTIC CONTAINER
MAGNESIUM SULFATE
2GM/100ML
INJECTABLE; INJECTION
Prescription
Yes
None
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