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"31722-595-32" National Drug Code (NDC)

Fenofibrate 100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-32)
(Camber Pharmaceuticals, Inc.)

NDC Code31722-595-32
Package Description100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-32)
Product NDC31722-595
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20160714
Marketing Category NameANDA
Application NumberANDA204598
ManufacturerCamber Pharmaceuticals, Inc.
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/31722-595-32





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