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"59651-617-08" National Drug Code (NDC)
Rufinamide 120 TABLET, FILM COATED in 1 BOTTLE (59651-617-08)
(Aurobindo Pharma Limited)
NDC Code
59651-617-08
Package Description
120 TABLET, FILM COATED in 1 BOTTLE (59651-617-08)
Product NDC
59651-617
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Rufinamide
Non-Proprietary Name
Rufinamide
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20230616
Marketing Category Name
ANDA
Application Number
ANDA217230
Manufacturer
Aurobindo Pharma Limited
Substance Name
RUFINAMIDE
Strength
400
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59651-617-08