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"61919-250-82" National Drug Code (NDC)

Glimepiride 180 TABLET in 1 BOTTLE (61919-250-82)
(DIRECT RX)

NDC Code61919-250-82
Package Description180 TABLET in 1 BOTTLE (61919-250-82)
Product NDC61919-250
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20160204
Marketing Category NameANDA
Application NumberANDA078181
ManufacturerDIRECT RX
Substance NameGLIMEPIRIDE
Strength4
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-250-82





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