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Cyclobenzaprine Hydrochloride - 0904-7809-61 - (Cyclobenzaprine Hydrochloride)

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Drug Information of Cyclobenzaprine Hydrochloride

Product NDC: 0904-7809
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: 0904-7809
Labeler Name: Major Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071611
Marketing Category: ANDA
Start Marketing Date: 19880229

Package Information of Cyclobenzaprine Hydrochloride

Package NDC: 0904-7809-61
Package Description: 100 TABLET in 1 BOX, UNIT-DOSE (0904-7809-61)

NDC Information of Cyclobenzaprine Hydrochloride

NDC Code 0904-7809-61
Proprietary Name Cyclobenzaprine Hydrochloride
Package Description 100 TABLET in 1 BOX, UNIT-DOSE (0904-7809-61)
Product NDC 0904-7809
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Cyclobenzaprine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880229
Marketing Category Name ANDA
Labeler Name Major Pharmaceuticals
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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