AMRIX - 54868-6022-0 - (Cyclobenzaprine Hydrochloride)

Alphabetical Index


Drug Information of AMRIX

Product NDC: 54868-6022
Proprietary Name: AMRIX
Non Proprietary Name: Cyclobenzaprine Hydrochloride
Active Ingredient(s): 15    mg/1 & nbsp;   Cyclobenzaprine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of AMRIX

Product NDC: 54868-6022
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021777
Marketing Category: NDA
Start Marketing Date: 20090416

Package Information of AMRIX

Package NDC: 54868-6022-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-6022-0)

NDC Information of AMRIX

NDC Code 54868-6022-0
Proprietary Name AMRIX
Package Description 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-6022-0)
Product NDC 54868-6022
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090416
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
Strength Number 15
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of AMRIX


General Information