"21695-037-21" National Drug Code (NDC)

Cyclobenzaprine Hydrochloride 21 TABLET in 1 BOTTLE (21695-037-21)
(Rebel Distributors)

NDC Code21695-037-21
Package Description21 TABLET in 1 BOTTLE (21695-037-21)
Product NDC21695-037
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCyclobenzaprine Hydrochloride
Non-Proprietary NameCyclobenzaprine Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20100218
Marketing Category NameANDA
Application NumberANDA078218
ManufacturerRebel Distributors
Substance NameCYCLOBENZAPRINE HYDROCHLORIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesCentrally-mediated Muscle Relaxation [PE],Muscle Relaxant [EPC]

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