DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
KETALAR
FDA Application No:
(NDA) 016812
Active Ingredient(s):
KETAMINE HYDROCHLORIDE
Company:
PARKEDALE
Original Approval or Tentative Approval Date:
February 19, 1970
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
Therapeutic Equivalents
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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
KETALAR
KETAMINE HYDROCHLORIDE
EQ 10MG BASE/ML
INJECTABLE; INJECTION
Prescription
Yes
None
KETALAR
KETAMINE HYDROCHLORIDE
EQ 50MG BASE/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
KETALAR
KETAMINE HYDROCHLORIDE
EQ 100MG BASE/ML
INJECTABLE; INJECTION
Prescription
Yes
AP
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