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"57664-441-18" National Drug Code (NDC)
Digoxin 1000 TABLET in 1 BOTTLE (57664-441-18)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
57664-441-18
Package Description
1000 TABLET in 1 BOTTLE (57664-441-18)
Product NDC
57664-441
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Digoxin
Non-Proprietary Name
Digoxin
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20150217
Marketing Category Name
ANDA
Application Number
ANDA076363
Manufacturer
Sun Pharmaceutical Industries, Inc.
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/57664-441-18