"43598-351-30" National Drug Code (NDC)

Lurasidone Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE (43598-351-30)
(Dr. Reddys Laboratories Inc)

NDC Code43598-351-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (43598-351-30)
Product NDC43598-351
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLurasidone Hydrochloride
Non-Proprietary NameLurasidone Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20230220
Marketing Category NameANDA
Application NumberANDA208047
ManufacturerDr. Reddys Laboratories Inc
Substance NameLURASIDONE HYDROCHLORIDE
Strength20
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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