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"63187-919-21" National Drug Code (NDC)
Famciclovir 21 TABLET in 1 BOTTLE (63187-919-21)
(Proficient Rx LP)
NDC Code
63187-919-21
Package Description
21 TABLET in 1 BOTTLE (63187-919-21)
Product NDC
63187-919
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famciclovir
Non-Proprietary Name
Famciclovir
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20110321
Marketing Category Name
ANDA
Application Number
ANDA078278
Manufacturer
Proficient Rx LP
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/63187-919-21