"72603-117-02" National Drug Code (NDC)

Glipizide 500 TABLET in 1 BOTTLE (72603-117-02)
(NorthStar RxLLC)

NDC Code72603-117-02
Package Description500 TABLET in 1 BOTTLE (72603-117-02)
Product NDC72603-117
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20230301
Marketing Category NameANDA
Application NumberANDA074550
ManufacturerNorthStar RxLLC
Substance NameGLIPIZIDE
Strength10
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

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