"52817-332-50" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (52817-332-50)
(TruPharma LLC)

NDC Code52817-332-50
Package Description500 TABLET, FILM COATED in 1 BOTTLE (52817-332-50)
Product NDC52817-332
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170531
Marketing Category NameANDA
Application NumberANDA208170
ManufacturerTruPharma LLC
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]

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