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"0115-1555-10" National Drug Code (NDC)

Fenofibric Acid 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1555-10)
(Amneal Pharmaceuticals of New York LLC)

NDC Code0115-1555-10
Package Description90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1555-10)
Product NDC0115-1555
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibric Acid
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20160912
End Marketing Date20260731
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022224
ManufacturerAmneal Pharmaceuticals of New York LLC
Substance NameFENOFIBRIC ACID
Strength135
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/0115-1555-10





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