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"23155-887-18" National Drug Code (NDC)

Lurasidone Hydrochloride 121000 TABLET, FILM COATED in 1 CONTAINER (23155-887-18)
(Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.)

NDC Code23155-887-18
Package Description121000 TABLET, FILM COATED in 1 CONTAINER (23155-887-18)
Product NDC23155-887
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
Strength20
Strength Unitmg/1
Pharmacy ClassesAtypical Antipsychotic [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/23155-887-18





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