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"69367-305-01" National Drug Code (NDC)
Miglitol 100 TABLET, COATED in 1 BOTTLE (69367-305-01)
(Westminster Pharmaceuticals, LLC)
NDC Code
69367-305-01
Package Description
100 TABLET, COATED in 1 BOTTLE (69367-305-01)
Product NDC
69367-305
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Miglitol
Non-Proprietary Name
Miglitol
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20210115
Marketing Category Name
ANDA
Application Number
ANDA203965
Manufacturer
Westminster Pharmaceuticals, LLC
Substance Name
MIGLITOL
Strength
100
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/69367-305-01