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: A073541
Product Number: 001
Approval Date: May 23, 1995
Applicant Holder Full Name: ANDA REPOSITORY LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
