"23155-891-18" National Drug Code (NDC)

Lurasidone Hydrochloride 20000 TABLET, FILM COATED in 1 CONTAINER (23155-891-18)
(Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.)

NDC Code23155-891-18
Package Description20000 TABLET, FILM COATED in 1 CONTAINER (23155-891-18)
Product NDC23155-891
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLurasidone Hydrochloride
Non-Proprietary NameLurasidone Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20231019
Marketing Category NameANDA
Application NumberANDA208058
ManufacturerHeritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.
Substance NameLURASIDONE HYDROCHLORIDE
Strength120
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

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