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"59762-7021-5" National Drug Code (NDC)

Glyburide 500 TABLET in 1 BOTTLE (59762-7021-5)
(Greenstone LLC)

NDC Code59762-7021-5
Package Description500 TABLET in 1 BOTTLE (59762-7021-5)
Product NDC59762-7021
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlyburide
Non-Proprietary NameGlyburide
Dosage FormTABLET
UsageORAL
Start Marketing Date20071018
End Marketing Date20140930
Marketing Category NameANDA
Application NumberANDA077537
ManufacturerGreenstone LLC
Substance NameGLYBURIDE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/59762-7021-5





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