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Cyclobenzaprine Hydrochloride - 10702-006-10 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 10702-006
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclobenzaprine Hydrochloride

Product NDC: 10702-006
Labeler Name: KVK-TECH, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078048
Marketing Category: ANDA
Start Marketing Date: 20120314

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 10702-006-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (10702-006-10)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 10702-006-10
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (10702-006-10)
Product NDC 10702-006
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120314
Marketing Category Name ANDA
Labeler Name KVK-TECH, 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


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