DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
HALDOL
FDA Application No:
(NDA) 018701
Active Ingredient(s):
HALOPERIDOL DECANOATE
Company:
ORTHO MCNEIL
Original Approval or Tentative Approval Date:
January 14, 1986
Chemical Type:
2 New active ingredient
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
HALDOL
HALOPERIDOL DECANOATE
EQ 50MG BASE/ML
INJECTABLE; INJECTION
Prescription
Yes
AO
HALDOL
HALOPERIDOL DECANOATE
EQ 100MG BASE/ML
INJECTABLE; INJECTION
Prescription
Yes
AO
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