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"70771-1735-4" National Drug Code (NDC)

Lurasidone Hydrochloride 10 BLISTER PACK in 1 CARTON (70771-1735-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1735-2)
(Zydus Lifesciences Limited)

NDC Code70771-1735-4
Package Description10 BLISTER PACK in 1 CARTON (70771-1735-4) / 10 TABLET, COATED in 1 BLISTER PACK (70771-1735-2)
Product NDC70771-1735
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLurasidone Hydrochloride
Non-Proprietary NameLurasidone Hydrochloride
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20230201
Marketing Category NameANDA
Application NumberANDA208052
ManufacturerZydus Lifesciences Limited
Substance NameLURASIDONE HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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