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Fenofibric acid

NDC 33342-295 · HUMAN PRESCRIPTION DRUG · CAPSULE, DELAYED RELEASE

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA207796
Dosage form / routeCAPSULE, DELAYED RELEASE · ORAL
Active ingredientsCHOLINE FENOFIBRATE (135 mg/1)
Marketing started20240226
Package count2

External sources

Source: openFDA. Public-domain (CC0).