"51655-143-83" National Drug Code (NDC)

Gemfibrozil 180 TABLET in 1 BOTTLE, PLASTIC (51655-143-83)
(Northwind Pharmaceuticals, LLC)

NDC Code51655-143-83
Package Description180 TABLET in 1 BOTTLE, PLASTIC (51655-143-83)
Product NDC51655-143
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20170814
Marketing Category NameANDA
Application NumberANDA077836
ManufacturerNorthwind Pharmaceuticals, LLC
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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