Active Ingredient: CYCLOBENZAPRINE HYDROCHLORIDE
Proprietary Name: CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A077797
Product Number: 001
Approval Date: Feb 28, 2007
Applicant Holder Full Name: PRINSTON PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information
Active Ingredient: CYCLOBENZAPRINE HYDROCHLORIDE
Proprietary Name: CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A077797
Product Number: 002
Approval Date: Feb 28, 2007
Applicant Holder Full Name: PRINSTON PHARMACEUTICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information