"70518-4039-0" National Drug Code (NDC)

Glimepiride 30 TABLET in 1 BLISTER PACK (70518-4039-0)
(REMEDYREPACK INC.)

NDC Code70518-4039-0
Package Description30 TABLET in 1 BLISTER PACK (70518-4039-0)
Product NDC70518-4039
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlimepiride
Non-Proprietary NameGlimepiride
Dosage FormTABLET
UsageORAL
Start Marketing Date20240319
Marketing Category NameANDA
Application NumberANDA202112
ManufacturerREMEDYREPACK INC.
Substance NameGLIMEPIRIDE
Strength2
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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