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"57664-745-18" National Drug Code (NDC)
Repaglinide 1000 TABLET in 1 BOTTLE (57664-745-18)
(Sun Pharmaceutical Industries, Inc.)
NDC Code
57664-745-18
Package Description
1000 TABLET in 1 BOTTLE (57664-745-18)
Product NDC
57664-745
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Repaglinide
Non-Proprietary Name
Repaglinide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20130711
Marketing Category Name
ANDA
Application Number
ANDA077571
Manufacturer
Sun Pharmaceutical Industries, Inc.
Substance Name
REPAGLINIDE
Strength
1
Strength Unit
mg/1
Pharmacy Classes
Glinide [EPC], Potassium Channel Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-745-18