"16571-774-50" National Drug Code (NDC)

Glimepiride 500 TABLET in 1 BOTTLE (16571-774-50)
(Rising Pharma Holdings, Inc.)

NDC Code16571-774-50
Package Description500 TABLET in 1 BOTTLE (16571-774-50)
Product NDC16571-774
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20120629
Marketing Category NameANDA
Application NumberANDA202759
ManufacturerRising Pharma Holdings, Inc.
Substance NameGLIMEPIRIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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