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"62332-351-90" National Drug Code (NDC)

Fenofibrate 90 TABLET, FILM COATED in 1 BOTTLE (62332-351-90)
(Alembic Pharmaceuticals Inc.)

NDC Code62332-351-90
Package Description90 TABLET, FILM COATED in 1 BOTTLE (62332-351-90)
Product NDC62332-351
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibrate
Non-Proprietary NameFenofibrate
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20200123
Marketing Category NameANDA
Application NumberANDA213252
ManufacturerAlembic Pharmaceuticals Inc.
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/62332-351-90





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