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"71205-949-30" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)
(Proficient Rx LP)

NDC Code71205-949-30
Package Description30 TABLET, FILM COATED in 1 BOTTLE (71205-949-30)
Product NDC71205-949
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200423
Marketing Category NameANDA
Application NumberANDA207803
ManufacturerProficient Rx LP
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/71205-949-30





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