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:
Application Number: A073143
Product Number: 001
Approval Date: Nov 27, 1991
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information