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"52817-332-00" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (52817-332-00)
(TruPharma LLC)

NDC Code52817-332-00
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (52817-332-00)
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]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52817-332-00





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