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"70436-169-03" National Drug Code (NDC)

Fenofibric Acid 500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-169-03)
(Slate Run Pharmaceuticals, LLC)

NDC Code70436-169-03
Package Description500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-169-03)
Product NDC70436-169
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
Strength135
Strength Unitmg/1
Pharmacy ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/70436-169-03





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