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"60687-666-21" National Drug Code (NDC)

Fenofibrate 30 BLISTER PACK in 1 CARTON (60687-666-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-666-11)
(American Health Packaging)

NDC Code60687-666-21
Package Description30 BLISTER PACK in 1 CARTON (60687-666-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-666-11)
Product NDC60687-666
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20221201
End Marketing Date20240229
Marketing Category NameANDA
Application NumberANDA076635
ManufacturerAmerican Health Packaging
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/60687-666-21





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