DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HYDASE
FDA Application No:
(NDA) 021716
Active Ingredient(s):
HYALURONIDASE
Company:
PRIMAPHARM
Original Approval or Tentative Approval Date:
October 25, 2005
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
HYDASE
HYALURONIDASE
150 UNITS/ML
INJECTABLE; INJECTION
Prescription
Yes
None
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