DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NUBAIN
FDA Application No:
(NDA) 018024
Active Ingredient(s):
NALBUPHINE HYDROCHLORIDE
Company:
ENDO PHARMS
Original Approval or Tentative Approval Date:
May 15, 1979
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard 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
NUBAIN
NALBUPHINE HYDROCHLORIDE
10MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
NUBAIN
NALBUPHINE HYDROCHLORIDE
20MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
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