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Cyclobenzaprine Hydrochloride - 50111-563-03 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 50111-563
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclobenzaprine Hydrochloride

Product NDC: 50111-563
Labeler Name: Pliva Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074421
Marketing Category: ANDA
Start Marketing Date: 19950929

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 50111-563-03
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (50111-563-03)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 50111-563-03
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (50111-563-03)
Product NDC 50111-563
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19950929
Marketing Category Name ANDA
Labeler Name Pliva Inc.
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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