Product Details for NDA 019835
ZYRTEC ALLERGY (CETIRIZINE HYDROCHLORIDE)
10MG
Marketing Status: Over-the-counter
5MG
Marketing Status: Discontinued
5MG
Marketing Status: Discontinued
10MG
Marketing Status: Discontinued
10MG
Marketing Status: Over-the-counter
Active Ingredient: CETIRIZINE HYDROCHLORIDE
Proprietary Name: ZYRTEC ALLERGY
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N019835
Product Number: 004
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Over-the-counter
Patent and Exclusivity Information
ZYRTEC ALLERGY (CETIRIZINE HYDROCHLORIDE)
Proprietary Name: ZYRTEC ALLERGY
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code:
Application Number: N019835
Product Number: 004
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Over-the-counter
Patent and Exclusivity Information
5MG
Marketing Status: Discontinued
Active Ingredient: CETIRIZINE HYDROCHLORIDE
Proprietary Name: ZYRTEC ALLERGY
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019835
Product Number: 003
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
ZYRTEC HIVES RELIEF (CETIRIZINE HYDROCHLORIDE)
Proprietary Name: ZYRTEC ALLERGY
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019835
Product Number: 003
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
5MG
Marketing Status: Discontinued
Active Ingredient: CETIRIZINE HYDROCHLORIDE
Proprietary Name: ZYRTEC HIVES RELIEF
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019835
Product Number: 005
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
ZYRTEC HIVES RELIEF (CETIRIZINE HYDROCHLORIDE)
Proprietary Name: ZYRTEC HIVES RELIEF
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019835
Product Number: 005
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
10MG
Marketing Status: Discontinued
Active Ingredient: CETIRIZINE HYDROCHLORIDE
Proprietary Name: ZYRTEC HIVES RELIEF
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019835
Product Number: 006
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: ZYRTEC HIVES RELIEF
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N019835
Product Number: 006
Approval Date: Nov 16, 2007
Applicant Holder Full Name: JOHNSON AND JOHNSON CONSUMER INC MCNEIL CONSUMER HEALTHCARE DIV
Marketing Status: Discontinued
Patent and Exclusivity Information