"52959-042-21" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 21 TABLET, FILM COATED in 1 CONTAINER (52959-042-21)
(H. J Harkins Company Inc)

NDC Code52959-042-21
Package Description21 TABLET, FILM COATED in 1 CONTAINER (52959-042-21)
Product NDC52959-042
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170103
Marketing Category NameANDA
Application NumberANDA077797
ManufacturerH. J Harkins Company Inc
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

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