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"70518-2308-0" National Drug Code (NDC)

Glipizide 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2308-0)
(REMEDYREPACK INC.)

NDC Code70518-2308-0
Package Description30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (70518-2308-0)
Product NDC70518-2308
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET, FILM COATED, EXTENDED RELEASE
UsageORAL
Start Marketing Date20190911
Marketing Category NameANDA
Application NumberANDA204720
ManufacturerREMEDYREPACK INC.
Substance NameGLIPIZIDE
Strength2.5
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70518-2308-0





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