Home > National Drug Code (NDC) > Cyclobenzaprine Hydrochloride

Cyclobenzaprine Hydrochloride - 50436-4842-1 - (cyclobenzaprine hydrochloride)

Alphabetical Index


Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 50436-4842
Proprietary Name: Cyclobenzaprine Hydrochloride
Non Proprietary Name: cyclobenzaprine hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   cyclobenzaprine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclobenzaprine Hydrochloride

Product NDC: 50436-4842
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077797
Marketing Category: ANDA
Start Marketing Date: 20070228

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 50436-4842-1
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (50436-4842-1)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 50436-4842-1
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (50436-4842-1)
Product NDC 50436-4842
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name cyclobenzaprine hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070228
Marketing Category Name ANDA
Labeler Name Unit Dose Services
Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Cyclobenzaprine Hydrochloride


General Information