DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NARCAN
FDA Application No:
(NDA) 016636
Active Ingredient(s):
NALOXONE HYDROCHLORIDE
Company:
ENDO PHARMS
Original Approval or Tentative Approval Date:
April 13, 1971
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
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
NARCAN
NALOXONE HYDROCHLORIDE
0.4MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
NARCAN
NALOXONE HYDROCHLORIDE
0.02MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
NARCAN
NALOXONE HYDROCHLORIDE
1MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
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