"61919-220-72" National Drug Code (NDC)

Tizanidine 120 TABLET in 1 BOTTLE (61919-220-72)
(Direct Rx)

NDC Code61919-220-72
Package Description120 TABLET in 1 BOTTLE (61919-220-72)
Product NDC61919-220
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTizanidine
Non-Proprietary NameTizanidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20140101
Marketing Category NameANDA
Application NumberANDA076533
ManufacturerDirect Rx
Substance NameTIZANIDINE HYDROCHLORIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

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