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: A077209
Product Number: 002
Approval Date: Feb 3, 2006
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
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: A077209
Product Number: 001
Approval Date: Oct 4, 2005
Applicant Holder Full Name: OXFORD PHARMACEUTICALS LLC
Marketing Status:
Prescription
Patent and Exclusivity Information