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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 011111

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VISTARIL (HYDROXYZINE HYDROCHLORIDE)
25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: HYDROXYZINE HYDROCHLORIDE
Proprietary Name: VISTARIL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N011111
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER LABORATORIES DIV PFIZER INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
VISTARIL (HYDROXYZINE HYDROCHLORIDE)
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
Active Ingredient: HYDROXYZINE HYDROCHLORIDE
Proprietary Name: VISTARIL
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N011111
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER LABORATORIES DIV PFIZER INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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