DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
OPANA
FDA Application No:
(NDA) 011707
Active Ingredient(s):
OXYMORPHONE HYDROCHLORIDE
Company:
ENDO PHARMS
Original Approval or Tentative Approval Date:
April 2, 1959
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
O Orphan drug
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
OPANA
OXYMORPHONE HYDROCHLORIDE
1.5MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
OPANA
OXYMORPHONE HYDROCHLORIDE
1MG/ML
INJECTABLE; INJECTION
Prescription
Yes
None
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