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"61919-722-30" National Drug Code (NDC)

Glipizide 30 TABLET in 1 BOTTLE (61919-722-30)
(DIRECT RX)

NDC Code61919-722-30
Package Description30 TABLET in 1 BOTTLE (61919-722-30)
Product NDC61919-722
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGlipizide
Non-Proprietary NameGlipizide
Dosage FormTABLET
UsageORAL
Start Marketing Date20181211
Marketing Category NameANDA
Application NumberANDA075795
ManufacturerDIRECT RX
Substance NameGLIPIZIDE
Strength5
Strength Unitmg/1
Pharmacy ClassesSulfonylurea Compounds [CS], Sulfonylurea [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/61919-722-30





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