"80175-0169-3" National Drug Code (NDC)

Tizanidine 30 TABLET in 1 BOTTLE (80175-0169-3)
(Central Packaging)

NDC Code80175-0169-3
Package Description30 TABLET in 1 BOTTLE (80175-0169-3)
Product NDC80175-0169
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTizanidine
Non-Proprietary NameTizanidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20130401
Marketing Category NameANDA
Application NumberANDA091283
ManufacturerCentral Packaging
Substance NameTIZANIDINE HYDROCHLORIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

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