"68071-4421-8" National Drug Code (NDC)

Gemfibrozil 180 TABLET in 1 BOTTLE (68071-4421-8)
(NuCare Pharmaceuticals,Inc.)

NDC Code68071-4421-8
Package Description180 TABLET in 1 BOTTLE (68071-4421-8)
Product NDC68071-4421
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20170215
Marketing Category NameANDA
Application NumberANDA203266
ManufacturerNuCare Pharmaceuticals,Inc.
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]

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