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Cyclobenzaprine Hydrochloride - 64376-177-61 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 64376-177
Proprietary Name: Cyclobenzaprine Hydrochloride
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 Cyclobenzaprine Hydrochloride

Product NDC: 64376-177
Labeler Name: Boca Pharmacal, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091281
Marketing Category: ANDA
Start Marketing Date: 20130131

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 64376-177-61
Package Description: 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (64376-177-61)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 64376-177-61
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (64376-177-61)
Product NDC 64376-177
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20130131
Marketing Category Name ANDA
Labeler Name Boca Pharmacal, 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 Cyclobenzaprine Hydrochloride


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