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"52125-972-23" National Drug Code (NDC)

Glipizide 180 TABLET in 1 BOTTLE (52125-972-23)
(REMEDYREPACK INC.)

NDC Code52125-972-23
Package Description180 TABLET in 1 BOTTLE (52125-972-23)
Product NDC52125-972
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20140616
Marketing Category NameANDA
Application NumberANDA077820
ManufacturerREMEDYREPACK INC.
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/52125-972-23





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