NDC 82009-060

Fenofibrate

Fenofibrate

Fenofibrate is a Oral Tablet, Coated in the Human Prescription Drug category. It is labeled and distributed by Quallent Pharmaceuticals Health Llc. The primary component is Fenofibrate.

Product ID82009-060_215a5000-9f89-47d9-b2d5-94e13f5e1767
NDC82009-060
Product TypeHuman Prescription Drug
Proprietary NameFenofibrate
Generic NameFenofibrate
Dosage FormTablet, Coated
Route of AdministrationORAL
Marketing Start Date2022-11-18
Marketing CategoryANDA /
Application NumberANDA205118
Labeler NameQUALLENT PHARMACEUTICALS HEALTH LLC
Substance NameFENOFIBRATE
Active Ingredient Strength145 mg/1
Pharm ClassesPeroxisome Proliferator Receptor alpha Agonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 82009-060-90

90 TABLET, COATED in 1 BOTTLE (82009-060-90)
Marketing Start Date2022-11-18
NDC Exclude FlagN
Sample Package?N

Drug Details