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"70518-1639-0" National Drug Code (NDC)

Glimepiride 90 TABLET in 1 BOTTLE, PLASTIC (70518-1639-0)
(REMEDYREPACK INC.)

NDC Code70518-1639-0
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70518-1639-0)
Product NDC70518-1639
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20181107
Marketing Category NameANDA
Application NumberANDA078181
ManufacturerREMEDYREPACK INC.
Substance NameGLIMEPIRIDE
Strength1
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [CS]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-1639-0





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