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"68462-713-30" National Drug Code (NDC)
Rufinamide 30 TABLET, FILM COATED in 1 BOTTLE (68462-713-30)
(Glenmark Pharmaceuticals Inc., USA)
NDC Code
68462-713-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (68462-713-30)
Product NDC
68462-713
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Rufinamide
Non-Proprietary Name
Rufinamide
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20160516
Marketing Category Name
ANDA
Application Number
ANDA205075
Manufacturer
Glenmark Pharmaceuticals Inc., USA
Substance Name
RUFINAMIDE
Strength
200
Strength Unit
mg/1
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68462-713-30