"70518-3504-0" National Drug Code (NDC)

Glyburide 30 TABLET in 1 BLISTER PACK (70518-3504-0)
(REMEDYREPACK INC.)

NDC Code70518-3504-0
Package Description30 TABLET in 1 BLISTER PACK (70518-3504-0)
Product NDC70518-3504
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlyburide
Non-Proprietary NameGlyburide
Dosage FormTABLET
UsageORAL
Start Marketing Date20220831
Marketing Category NameANDA
Application NumberANDA203379
ManufacturerREMEDYREPACK INC.
Substance NameGLYBURIDE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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