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"70518-4132-0" National Drug Code (NDC)

Lurasidone Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4132-0)
(REMEDYREPACK INC.)

NDC Code70518-4132-0
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4132-0)
Product NDC70518-4132
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLurasidone Hydrochloride
Non-Proprietary NameLurasidone Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20240701
Marketing Category NameANDA
Application NumberANDA208047
ManufacturerREMEDYREPACK INC.
Substance NameLURASIDONE HYDROCHLORIDE
Strength80
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-4132-0





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