Fenofibrate Capsule
Product Images NDC 62332-084

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 62332-084). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Fenofibrate 134mg

Label for Fenofibrate Capsules, USP 134 mg by Alembic Pharmaceuticals Inc. The label states the active ingredient is fenofibrate (micronized) 134 mg per capsule, provided in a 30-capsule package. It includes storage instructions, a caution not to use if the seal is broken, and that the package is child-resistant. The label also shows the NDC 62332-085-30 and barcode.*

FDA Label Image

Fenofibrate 200mg

Label for Fenofibrate Capsules, USP 200 mg, oral capsules supplied by Alembic Pharmaceuticals Inc. The label indicates 30 capsules per package and features dosage instructions, storage conditions, and child-resistant packaging information, along with barcode and lot number sections.*

FDA Label Image

Fenofibrate 67mg

Label for Fenofibrate Capsules, USP 67 mg from Alembic Pharmaceuticals Inc. It shows prescription capsules in a 30-count package. The label includes dosage strength, storage instructions, barcode, and manufacturer details. The capsule is child-resistant and includes caution not to use if the seal is broken or missing.*

FDA Label Image

Fenofibrate-structure (Fenofibrate Structure)

Chemical structure of fenofibrate, showing molecular bonds and arrangement of functional groups including chlorine, aromatic rings, ester, and carbonyl groups.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.