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CYCLOBENZAPRINE HYROCHLORIDE - 76519-1000-2 - (CYCLOBENZAPRINE HYDROCHLORIDE)

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Drug Information of CYCLOBENZAPRINE HYROCHLORIDE

Product NDC: 76519-1000
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: 76519-1000
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078722
Marketing Category: ANDA
Start Marketing Date: 20110829

Package Information of CYCLOBENZAPRINE HYROCHLORIDE

Package NDC: 76519-1000-2
Package Description: 20 TABLET in 1 BOTTLE (76519-1000-2)

NDC Information of CYCLOBENZAPRINE HYROCHLORIDE

NDC Code 76519-1000-2
Proprietary Name CYCLOBENZAPRINE HYROCHLORIDE
Package Description 20 TABLET in 1 BOTTLE (76519-1000-2)
Product NDC 76519-1000
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 H.J. Harkins Company, Inc.
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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