FDA Drug Application (078722) for CYCLOBENZAPRINE HYDROCHLORIDE by SUN PHARM INDS LTD

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Application Number078722
Product Number001
FormTABLET;ORAL
Dosage5MG
Product Market Status Prescription
Therapeutic Equivalence Evaluation Code AB Products meeting necessary bioequivalence requirements
Reference Drug
Drug NameCYCLOBENZAPRINE HYDROCHLORIDE
Active IngredientCYCLOBENZAPRINE HYDROCHLORIDE

Active IngredientCount
List of drugs with Active Ingredient CYCLOBENZAPRINE HYDROCHLORIDE3


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