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"57664-399-13" National Drug Code (NDC)

Glipizide 500 TABLET in 1 BOTTLE (57664-399-13)
(Sun Pharmaceutical Industries, Inc.)

NDC Code57664-399-13
Package Description500 TABLET in 1 BOTTLE (57664-399-13)
Product NDC57664-399
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20090731
Marketing Category NameANDA
Application NumberANDA077820
ManufacturerSun Pharmaceutical Industries, Inc.
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/57664-399-13





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