"61919-065-20" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 20 TABLET in 1 BOTTLE (61919-065-20)
(Direct Rx)

NDC Code61919-065-20
Package Description20 TABLET in 1 BOTTLE (61919-065-20)
Product NDC61919-065
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA090478
ManufacturerDirect Rx
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

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