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"67046-1361-3" National Drug Code (NDC)

Fenofibrate 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1361-3)
(Coupler LLC)

NDC Code67046-1361-3
Package Description30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1361-3)
Product NDC67046-1361
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20241112
Marketing Category NameANDA
Application NumberANDA204598
ManufacturerCoupler LLC
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/67046-1361-3





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