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"65862-769-78" National Drug Code (NDC)

Fenofibrate 10 BLISTER PACK in 1 CARTON (65862-769-78) > 10 TABLET, COATED in 1 BLISTER PACK (65862-769-10)
(Aurobindo Pharma Limited)

NDC Code65862-769-78
Package Description10 BLISTER PACK in 1 CARTON (65862-769-78) > 10 TABLET, COATED in 1 BLISTER PACK (65862-769-10)
Product NDC65862-769
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, COATED
UsageORAL
Start Marketing Date20160505
Marketing Category NameANDA
Application NumberANDA205118
ManufacturerAurobindo Pharma Limited
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/65862-769-78





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