"57664-502-18" National Drug Code (NDC)

Tizanidine 1000 TABLET in 1 BOTTLE (57664-502-18)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-502-18
Package Description1000 TABLET in 1 BOTTLE (57664-502-18)
Product NDC57664-502
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameTizanidine
Non-Proprietary NameTizanidine
Dosage FormTABLET
UsageORAL
Start Marketing Date20031211
Marketing Category NameANDA
Application NumberANDA076416
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameTIZANIDINE HYDROCHLORIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesAdrenergic alpha2-Agonists [MoA], Central alpha-2 Adrenergic Agonist [EPC]

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