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"0093-8119-56" National Drug Code (NDC)
Famciclovir 30 TABLET, FILM COATED in 1 BOTTLE (0093-8119-56)
(Teva Pharmaceuticals USA, Inc.)
NDC Code
0093-8119-56
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (0093-8119-56)
Product NDC
0093-8119
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famciclovir
Non-Proprietary Name
Famciclovir
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20070905
Marketing Category Name
ANDA
Application Number
ANDA077487
Manufacturer
Teva Pharmaceuticals USA, Inc.
Substance Name
FAMCICLOVIR
Strength
500
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/0093-8119-56