DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HALOPERIDOL DECANOATE
FDA Application No:
(ANDA) 075176
Active Ingredient(s):
HALOPERIDOL DECANOATE
Company:
HOSPIRA
Original Approval or Tentative Approval Date:
February 9, 2000
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
HALOPERIDOL DECANOATE
HALOPERIDOL DECANOATE
EQ 50MG BASE/ML
INJECTABLE; INJECTION
Discontinued
No
None
HALOPERIDOL DECANOATE
HALOPERIDOL DECANOATE
EQ 100MG BASE/ML
INJECTABLE; INJECTION
Discontinued
No
None
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