DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
MAGNESIUM SULFATE
FDA Application No:
(ANDA) 075151
Active Ingredient(s):
MAGNESIUM SULFATE
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
April 25, 2000
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
MAGNESIUM SULFATE
MAGNESIUM SULFATE
500MG/ML
INJECTABLE; INJECTION
Prescription
No
AP
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