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"71205-935-30" National Drug Code (NDC)

Miglitol 30 TABLET, COATED in 1 BOTTLE (71205-935-30)
(Proficient Rx LP)

NDC Code71205-935-30
Package Description30 TABLET, COATED in 1 BOTTLE (71205-935-30)
Product NDC71205-935
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameMiglitol
Non-Proprietary NameMiglitol
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20210115
Marketing Category NameANDA
Application NumberANDA203965
ManufacturerProficient Rx LP
Substance NameMIGLITOL
Strength25
Strength Unitmg/1
Pharmacy Classesalpha Glucosidase Inhibitors [MoA], alpha-Glucosidase Inhibitor [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71205-935-30





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