Product Details for NDA 011111
VISTARIL (HYDROXYZINE HYDROCHLORIDE)
25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Marketing Status: Discontinued
25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Strength: 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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)
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Strength: 25MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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Strength: 50MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
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