"69844-013-02" National Drug Code (NDC)

Fenofibrate 90 TABLET in 1 BOTTLE (69844-013-02)
(Graviti Pharmaceuticals Private Limited)

NDC Code69844-013-02
Package Description90 TABLET in 1 BOTTLE (69844-013-02)
Product NDC69844-013
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20200318
Marketing Category NameANDA
Application NumberANDA211122
ManufacturerGraviti Pharmaceuticals Private Limited
Substance NameFENOFIBRATE
Strength145
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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