Home > National Drug Code (NDC) > cyclobenzaprine hydrochloride

cyclobenzaprine hydrochloride - 59746-211-10 - (cyclobenzaprine hydrochloride)

Alphabetical Index


Drug Information of cyclobenzaprine hydrochloride

Product NDC: 59746-211
Proprietary Name: cyclobenzaprine hydrochloride
Non Proprietary Name: cyclobenzaprine hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   cyclobenzaprine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of cyclobenzaprine hydrochloride

Product NDC: 59746-211
Labeler Name: JUBILANT CADISTA PHARMACEUTICALS, INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077563
Marketing Category: ANDA
Start Marketing Date: 20060404

Package Information of cyclobenzaprine hydrochloride

Package NDC: 59746-211-10
Package Description: 1000 TABLET in 1 BOTTLE (59746-211-10)

NDC Information of cyclobenzaprine hydrochloride

NDC Code 59746-211-10
Proprietary Name cyclobenzaprine hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (59746-211-10)
Product NDC 59746-211
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cyclobenzaprine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060404
Marketing Category Name ANDA
Labeler Name JUBILANT CADISTA PHARMACEUTICALS, INC.
Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of cyclobenzaprine hydrochloride


General Information