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"23155-891-10" National Drug Code (NDC)
Lurasidone Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (23155-891-10)
(Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.)
NDC Code
23155-891-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (23155-891-10)
Product NDC
23155-891
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Lurasidone Hydrochloride
Non-Proprietary Name
Lurasidone Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20231019
Marketing Category Name
ANDA
Application Number
ANDA208058
Manufacturer
Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Inc.
Substance Name
LURASIDONE HYDROCHLORIDE
Strength
120
Strength Unit
mg/1
Pharmacy Classes
Atypical Antipsychotic [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/23155-891-10