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"60687-103-21" National Drug Code (NDC)
Famciclovir 30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-103-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-103-11)
(American Health Packaging)
NDC Code
60687-103-21
Package Description
30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-103-21) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-103-11)
Product NDC
60687-103
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Famciclovir
Non-Proprietary Name
Famciclovir
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150331
Marketing Category Name
ANDA
Application Number
ANDA091480
Manufacturer
American Health Packaging
Substance Name
FAMCICLOVIR
Strength
500
Strength Unit
mg/1
Pharmacy Classes
DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/60687-103-21