"70436-168-03" National Drug Code (NDC)

Fenofibric Acid 1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-168-03)
(Slate Run Pharmaceuticals, LLC)

NDC Code70436-168-03
Package Description1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-168-03)
Product NDC70436-168
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameFenofibric Acid
Non-Proprietary NameFenofibric Acid
Dosage FormCAPSULE, DELAYED RELEASE
UsageORAL
Start Marketing Date20220411
Marketing Category NameANDA
Application NumberANDA212562
ManufacturerSlate Run Pharmaceuticals, LLC
Substance NameFENOFIBRIC ACID
Strength45
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

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