High Outlier
Strength
15 mg/1
Manufacturer
Teva Pharmaceuticals USA Inc.NDC
00093192006
Classification
Generic
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
CYCLOBENZAPRINE HYDROCHLORIDEApproval Type
Authorized Generic (NDA)
FDA Application
NDA021777On Market Since
3/4/2019
Pharmacological Classes
Centrally-mediated Muscle Relaxation
Muscle Relaxant
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