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"70518-4117-0" National Drug Code (NDC)
Lurasidone Hydrochloride 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4117-0)
(REMEDYREPACK INC.)
NDC Code
70518-4117-0
Package Description
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4117-0)
Product NDC
70518-4117
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
20240627
Marketing Category Name
ANDA
Application Number
ANDA208047
Manufacturer
REMEDYREPACK INC.
Substance Name
LURASIDONE HYDROCHLORIDE
Strength
40
Strength Unit
mg/1
Pharmacy Classes
Atypical Antipsychotic [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-4117-0