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"61919-723-90" National Drug Code (NDC)

Glimepiride 90 TABLET in 1 BOTTLE (61919-723-90)
(DIRECT RX)

NDC Code61919-723-90
Package Description90 TABLET in 1 BOTTLE (61919-723-90)
Product NDC61919-723
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20181219
Marketing Category NameANDA
Application NumberANDA078181
ManufacturerDIRECT RX
Substance NameGLIMEPIRIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-723-90





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