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Cyclobenzaprine Hydrochloride - 49349-891-02 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 49349-891
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: 49349-891
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078218
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 49349-891-02
Package Description: 30 TABLET in 1 VIAL (49349-891-02)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 49349-891-02
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 30 TABLET in 1 VIAL (49349-891-02)
Product NDC 49349-891
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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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