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Cyclobenzaprine Hydrochloride - 21695-036-78 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 21695-036
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
Coding System: National Drug Codes(NDC)

Labeler Information of Cyclobenzaprine Hydrochloride

Product NDC: 21695-036
Labeler Name: Rebel Distributors
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077563
Marketing Category: ANDA
Start Marketing Date: 20060419

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 21695-036-78
Package Description: 180 TABLET in 1 BOTTLE (21695-036-78)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 21695-036-78
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 180 TABLET in 1 BOTTLE (21695-036-78)
Product NDC 21695-036
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060419
Marketing Category Name ANDA
Labeler Name Rebel Distributors
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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