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"65862-670-99" National Drug Code (NDC)
Repaglinide 1000 TABLET in 1 BOTTLE (65862-670-99)
(Aurobindo Pharma Limited)
NDC Code
65862-670-99
Package Description
1000 TABLET in 1 BOTTLE (65862-670-99)
Product NDC
65862-670
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Repaglinide
Non-Proprietary Name
Repaglinide
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20140122
Marketing Category Name
ANDA
Application Number
ANDA203820
Manufacturer
Aurobindo Pharma Limited
Substance Name
REPAGLINIDE
Strength
.5
Strength Unit
mg/1
Pharmacy Classes
Glinide [EPC], Potassium Channel Antagonists [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/65862-670-99