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CYCLOBENZAPRINE HYROCHLORIDE - 63629-4664-4 - (CYCLOBENZAPRINE HYDROCHLORIDE)

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Drug Information of CYCLOBENZAPRINE HYROCHLORIDE

Product NDC: 63629-4664
Proprietary Name: CYCLOBENZAPRINE HYROCHLORIDE
Non Proprietary Name: CYCLOBENZAPRINE HYDROCHLORIDE
Active Ingredient(s): 7.5    mg/1 & nbsp;   CYCLOBENZAPRINE HYDROCHLORIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of CYCLOBENZAPRINE HYROCHLORIDE

Product NDC: 63629-4664
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078722
Marketing Category: ANDA
Start Marketing Date: 20110829

Package Information of CYCLOBENZAPRINE HYROCHLORIDE

Package NDC: 63629-4664-4
Package Description: 120 TABLET in 1 BOTTLE (63629-4664-4)

NDC Information of CYCLOBENZAPRINE HYROCHLORIDE

NDC Code 63629-4664-4
Proprietary Name CYCLOBENZAPRINE HYROCHLORIDE
Package Description 120 TABLET in 1 BOTTLE (63629-4664-4)
Product NDC 63629-4664
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name CYCLOBENZAPRINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110829
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
Strength Number 7.5
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of CYCLOBENZAPRINE HYROCHLORIDE


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