DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ESCITALOPRAM OXALATE
FDA Application No:
(ANDA) 077660
Active Ingredient(s):
ESCITALOPRAM OXALATE
Company:
ALPHAPHARM
Original Approval or Tentative Approval Date:
July 31, 2007
There are no 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
ESCITALOPRAM OXALATE
ESCITALOPRAM OXALATE
EQ 5MG BASE
CAPSULE; ORAL
Prescription
No
None
ESCITALOPRAM OXALATE
ESCITALOPRAM OXALATE
EQ 10MG BASE
CAPSULE; ORAL
Prescription
No
None
ESCITALOPRAM OXALATE
ESCITALOPRAM OXALATE
EQ 20MG BASE
CAPSULE; ORAL
Prescription
Yes
None
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