DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
DESFERAL
FDA Application No:
(NDA) 016267
Active Ingredient(s):
DEFEROXAMINE MESYLATE
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
April 1, 1968
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
Therapeutic Equivalents
Label Information
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
DESFERAL
DEFEROXAMINE MESYLATE
500MG/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
DESFERAL
DEFEROXAMINE MESYLATE
2GM/VIAL
INJECTABLE; INJECTION
Prescription
Yes
AP
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