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"69844-012-03" National Drug Code (NDC)

Fenofibrate 1000 TABLET in 1 BOTTLE (69844-012-03)
(Graviti Pharmaceuticals Private Limited)

NDC Code69844-012-03
Package Description1000 TABLET in 1 BOTTLE (69844-012-03)
Product NDC69844-012
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
Strength48
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69844-012-03





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