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"57664-685-88" National Drug Code (NDC)
Miglitol 100 TABLET, COATED in 1 BOTTLE (57664-685-88)
(Sun Pharmaceutical Industries Inc.)
NDC Code
57664-685-88
Package Description
100 TABLET, COATED in 1 BOTTLE (57664-685-88)
Product NDC
57664-685
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Miglitol
Non-Proprietary Name
Miglitol
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20160104
Marketing Category Name
ANDA
Application Number
ANDA203965
Manufacturer
Sun Pharmaceutical Industries Inc.
Substance Name
MIGLITOL
Strength
50
Strength Unit
mg/1
Pharmacy Classes
alpha Glucosidase Inhibitors [MoA], alpha-Glucosidase Inhibitor [EPC]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-685-88