DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IFSOFAMIDE
FDA Application No:
(ANDA) 076657
Active Ingredient(s):
IFOSFAMIDE
Company:
TEVA PARENTERAL
Original Approval or Tentative Approval Date:
April 4, 2007
There are no Therapeutic Equivalents
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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
IFSOFAMIDE
IFOSFAMIDE
1GM/20ML (50MG/ML)
INJECTABLE; INJECTION
Prescription
Yes
None
IFSOFAMIDE
IFOSFAMIDE
3GM/60ML (50MG/ML)
INJECTABLE; INJECTION
Prescription
Yes
None
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