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"71335-0159-1" National Drug Code (NDC)
Digoxin 30 TABLET in 1 BOTTLE (71335-0159-1)
(Bryant Ranch Prepack)
NDC Code
71335-0159-1
Package Description
30 TABLET in 1 BOTTLE (71335-0159-1)
Product NDC
71335-0159
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Digoxin
Non-Proprietary Name
Digoxin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20020726
Marketing Category Name
ANDA
Application Number
ANDA076268
Manufacturer
Bryant Ranch Prepack
Substance Name
DIGOXIN
Strength
250
Strength Unit
ug/1
Pharmacy Classes
Cardiac Glycoside [EPC],Cardiac Glycosides [CS]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0159-1