DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
RETAVASE
FDA Application No:
(BLA) 103786
Active Ingredient(s):
RETEPLASE
Company:
CENTOCOR INC
Original Approval or Tentative Approval Date:
October 30, 1996
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
RETAVASE
RETEPLASE
18.8MG/VIAL
VIAL
Prescription
No
None
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