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"76333-125-12" National Drug Code (NDC)
Miglitol 1000 TABLET, COATED in 1 BOTTLE (76333-125-12)
(Orient Pharma Co., Ltd.)
NDC Code
76333-125-12
Package Description
1000 TABLET, COATED in 1 BOTTLE (76333-125-12)
Product NDC
76333-125
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Miglitol
Non-Proprietary Name
Miglitol
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20150731
Marketing Category Name
ANDA
Application Number
ANDA203965
Manufacturer
Orient Pharma Co., Ltd.
Substance Name
MIGLITOL
Strength
25
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/76333-125-12