DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
VISTARIL
FDA Application No:
(NDA) 011459
Active Ingredient(s):
HYDROXYZINE PAMOATE
Company:
PFIZER
Original Approval or Tentative Approval Date:
November 15, 1968
Chemical Type:
2 New active ingredient
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
VISTARIL
HYDROXYZINE PAMOATE
EQ 25MG HCL
CAPSULE; ORAL
Prescription
No
AB
VISTARIL
HYDROXYZINE PAMOATE
EQ 50MG HCL
CAPSULE; ORAL
Prescription
Yes
AB
VISTARIL
HYDROXYZINE PAMOATE
EQ 100MG HCL
CAPSULE; ORAL
Discontinued
No
None
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