"70914-011-30" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (70914-011-30)
(Hudson Scientific LLC)

NDC Code70914-011-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (70914-011-30)
Product NDC70914-011
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20170104
Marketing Category NameANDA
Application NumberANDA090478
ManufacturerHudson Scientific LLC
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

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