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"16714-101-05" National Drug Code (NDC)

Gemfibrozil 500 TABLET in 1 BOTTLE (16714-101-05)
(Northstar RxLLC)

NDC Code16714-101-05
Package Description500 TABLET in 1 BOTTLE (16714-101-05)
Product NDC16714-101
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameGemfibrozil
Non-Proprietary NameGemfibrozil
Dosage FormTABLET
UsageORAL
Start Marketing Date20101220
End Marketing Date20260630
Marketing Category NameANDA
Application NumberANDA079072
ManufacturerNorthstar RxLLC
Substance NameGEMFIBROZIL
Strength600
Strength Unitmg/1
Pharmacy ClassesPPAR alpha [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator-activated Receptor alpha Agonists [MoA]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/16714-101-05





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