"70934-255-90" National Drug Code (NDC)

Gemfibrozil 90 TABLET in 1 BOTTLE, PLASTIC (70934-255-90)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)

NDC Code70934-255-90
Package Description90 TABLET in 1 BOTTLE, PLASTIC (70934-255-90)
Product NDC70934-255
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20190122
End Marketing Date20240331
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerDenton Pharma, Inc. DBA Northwind Pharmaceuticals
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]

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