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"16714-615-01" National Drug Code (NDC)
Famciclovir 30 TABLET in 1 BOTTLE (16714-615-01)
(NorthStar RxLLC)
NDC Code
16714-615-01
Package Description
30 TABLET in 1 BOTTLE (16714-615-01)
Product NDC
16714-615
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famciclovir
Non-Proprietary Name
Famciclovir
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20170201
Marketing Category Name
ANDA
Application Number
ANDA078278
Manufacturer
NorthStar RxLLC
Substance Name
FAMCICLOVIR
Strength
250
Strength Unit
mg/1
Pharmacy Classes
DNA Polymerase Inhibitors [MoA], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-615-01