"47335-578-13" National Drug Code (NDC)

Lurasidone Hydrochloride 500 TABLET in 1 BOTTLE (47335-578-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code47335-578-13
Package Description500 TABLET in 1 BOTTLE (47335-578-13)
Product NDC47335-578
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLurasidone Hydrochloride
Non-Proprietary NameLurasidone Hydrochloride
Dosage FormTABLET
UsageORAL
Start Marketing Date20230220
Marketing Category NameANDA
Application NumberANDA208066
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameLURASIDONE HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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