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Cyclobenzaprine Hydrochloride - 63629-1339-5 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 63629-1339
Proprietary Name: Cyclobenzaprine Hydrochloride
Non Proprietary Name: Cyclobenzaprine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Cyclobenzaprine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclobenzaprine Hydrochloride

Product NDC: 63629-1339
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078218
Marketing Category: ANDA
Start Marketing Date: 20100218

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 63629-1339-5
Package Description: 15 TABLET in 1 BOTTLE (63629-1339-5)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 63629-1339-5
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 15 TABLET in 1 BOTTLE (63629-1339-5)
Product NDC 63629-1339
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100218
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Cyclobenzaprine Hydrochloride


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