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"71335-0039-6" National Drug Code (NDC)

Glipizide 20 TABLET in 1 BOTTLE (71335-0039-6)
(Bryant Ranch Prepack)

NDC Code71335-0039-6
Package Description20 TABLET in 1 BOTTLE (71335-0039-6)
Product NDC71335-0039
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20110718
Marketing Category NameANDA
Application NumberANDA074550
ManufacturerBryant Ranch Prepack
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/71335-0039-6





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