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Cyclobenzaprine Hydrochloride - 63739-066-10 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 63739-066
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: 63739-066
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071611
Marketing Category: ANDA
Start Marketing Date: 20070614

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 63739-066-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-066-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 63739-066-10
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-066-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-066
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070614
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
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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