AMRIX - 21695-723-28 - (Cyclobenzaprine Hydrochloride)

Alphabetical Index


Drug Information of AMRIX

Product NDC: 21695-723
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: 21695-723
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021777
Marketing Category: NDA
Start Marketing Date: 20071001

Package Information of AMRIX

Package NDC: 21695-723-28
Package Description: 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-723-28)

NDC Information of AMRIX

NDC Code 21695-723-28
Proprietary Name AMRIX
Package Description 28 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (21695-723-28)
Product NDC 21695-723
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20071001
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp.
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