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"0115-1325-10" National Drug Code (NDC)

Fenofibric Acid 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1325-10)
(Amneal Pharmaceuticals of New York LLC)

NDC Code0115-1325-10
Package Description90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1325-10)
Product NDC0115-1325
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibric Acid
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20240601
Marketing Category NameANDA
Application NumberANDA200264
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/0115-1325-10





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