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Cyclobenzaprine Hydrochloride - 0781-5032-01 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 0781-5032
Proprietary Name: Cyclobenzaprine Hydrochloride
Non Proprietary Name: Cyclobenzaprine Hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   Cyclobenzaprine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclobenzaprine Hydrochloride

Product NDC: 0781-5032
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072854
Marketing Category: ANDA
Start Marketing Date: 20060206

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 0781-5032-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0781-5032-01)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 0781-5032-01
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0781-5032-01)
Product NDC 0781-5032
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20060206
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CYCLOBENZAPRINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Centrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

Complete Information of Cyclobenzaprine Hydrochloride


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