"49349-719-02" National Drug Code (NDC)

Glipizide 30 TABLET in 1 BLISTER PACK (49349-719-02)
(REMEDYREPACK INC.)

NDC Code49349-719-02
Package Description30 TABLET in 1 BLISTER PACK (49349-719-02)
Product NDC49349-719
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20110511
Marketing Category NameANDA
Application NumberANDA074223
ManufacturerREMEDYREPACK INC.
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea [EPC],Sulfonylurea Compounds [Chemical/Ingredient]

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