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"71335-2110-1" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 14 TABLET, FILM COATED in 1 BOTTLE (71335-2110-1)
(Bryant Ranch Prepack)

NDC Code71335-2110-1
Package Description14 TABLET, FILM COATED in 1 BOTTLE (71335-2110-1)
Product NDC71335-2110
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20080926
Marketing Category NameANDA
Application NumberANDA078643
ManufacturerBryant Ranch Prepack
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/71335-2110-1





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