Fenofibric Acid Capsule, Delayed Release
Product Images NDC 62332-244

3 FDA label images from Alembic Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Fenofibric Acid (NDC 62332-244). 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

Fenofibric mg135

Fenofibric mg135
Fenofibric Acid delayed-release capsules, 135 mg strength, oral dosage form, presented in a 30-capsule package. The label shows NDC 62332-245-30 and is labeled for prescription use only. Manufactured by Alembic Pharmaceuticals Inc., with manufacturing locations in Gujarat, India, and Bedminster, NJ, USA. The label includes storage instructions and a barcode.*
FDA Label Image

Fenofibric mg45

Fenofibric mg45
Fenofibric Acid 45 mg delayed-release capsules label for oral use. The label states the capsules contain choline fenofebrate equivalent to 45 mg fenofibric acid, with 30 capsules in the package. Manufactured by Alembic Pharmaceuticals and Alembic Pharmaceuticals Inc. The label also includes the NDC 62332-244-30, barcode, handling instructions, and branding for Alembic.*
FDA Label Image

Structure (Fenofibricacid Str)

Structure (Fenofibricacid Str)
Chemical structure of fenofibric acid, showing its molecular components including aromatic rings, chlorine atom, and carboxylate group complexed with a positively charged nitrogen-containing moiety.*

* 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.