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"68382-232-16" National Drug Code (NDC)

Fenofibric Acid 90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-232-16)
(Zydus Pharmaceuticals USA Inc)

NDC Code68382-232-16
Package Description90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68382-232-16)
Product NDC68382-232
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibric Acid
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20160912
Marketing Category NameNDA AUTHORIZED GENERIC
Application NumberNDA022224
ManufacturerZydus Pharmaceuticals USA Inc
Substance NameFENOFIBRIC ACID
Strength45
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-232-16





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