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"69844-009-01" National Drug Code (NDC)

Fenofibrate 30 TABLET in 1 BOTTLE (69844-009-01)
(Graviti Pharmaceuticals Private Limited)

NDC Code69844-009-01
Package Description30 TABLET in 1 BOTTLE (69844-009-01)
Product NDC69844-009
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Proprietary Name SuffixFilm Coated
Non-Proprietary NameFenofibrate
Dosage FormTABLET
UsageORAL
Start Marketing Date20180817
Marketing Category NameANDA
Application NumberANDA210606
ManufacturerGraviti Pharmaceuticals Private Limited
Substance NameFENOFIBRATE
Strength160
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/69844-009-01





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