DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
Rebif
FDA Application No:
(BLA) 103780
Active Ingredient(s):
Interferon beta-1a
Company:
SERONO INC
Original Approval or Tentative Approval Date:
March 7, 2002
There are no 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
Rebif
Interferon beta-1a
22UG/0.5ML
SYRINGE
Prescription
No
None
Rebif
Interferon beta-1a
44UG/0.5ML
SYRINGE
Prescription
No
None
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