Strength
5 mg/1
Manufacturer
Rising Pharma Holdings Inc.NDC
16571078201
Classification
Generic
Dosage Form
TABLET, FILM COATED
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
CYCLOBENZAPRINE HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA078643On Market Since
9/26/2008
Pharmacological Classes
Centrally-mediated Muscle Relaxation
Muscle Relaxant
CYCLOBENZAPRINE 5 MG TABLET
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