"55700-229-21" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-229-21)
(Lake Erie Medical DBA Quality Care Products LLC)

NDC Code55700-229-21
Package Description21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55700-229-21)
Product NDC55700-229
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20070228
Marketing Category NameANDA
Application NumberANDA077797
ManufacturerLake Erie Medical DBA Quality Care Products LLC
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

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