Fenofibrate Tablet, Film Coated
Product Images NDC 31722-596

8 FDA label images from Camber Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Fenofibrate (NDC 31722-596). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber 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

Fenofibrate145mg30s (Fenofibrate145mg30s)

Fenofibrate145mg30s (Fenofibrate145mg30s)
Fenofibrate Tablets USP 145 mg film-coated tablet label from Camber Pharmaceuticals, Inc. The label includes storage instructions, a barcode, and notes that the bottle contains 30 tablets. The product is specified as prescription only and manufactured for Camber Pharmaceuticals, Inc., with additional manufacturing by Hetero Labs Limited in Hyderabad, India.*
FDA Label Image

Fenofibrate145mgcarton (Fenofibrate145mgcarton)

Fenofibrate145mgcarton (Fenofibrate145mgcarton)
Packaging label for Fenofibrate Tablets, USP 145 mg film-coated tablets by Camber Pharmaceuticals, Inc. The label includes the NDC 31722-596-32 and indicates a package size of 100 unit dose tablets (10 x 10). It is marked Rx Only and includes manufacturer details for Hetero Labs Limited and Camber Pharmaceuticals, Inc.*
FDA Label Image

Fenofibrate145mgfoil (Fenofibrate145mgfoil)

Fenofibrate145mgfoil (Fenofibrate145mgfoil)
Fenofibrate Tablet, USP 145 mg film-coated tablets, shown as a strip of five labels each with a barcode, NDC 31722-596-32, and storage instruction to protect from moisture. Labels state manufacture by Camber Pharmaceuticals, Inc., with packaging for Hetero Labs Limited. Each label includes expiration date placeholder.*
FDA Label Image

Fenofibrate48mg30s (Fenofibrate48mg30s)

Fenofibrate48mg30s (Fenofibrate48mg30s)
Packaging label for Fenofibrate Tablets, USP 48 mg, film-coated oral tablets. The label shows the product strength (48 mg) prominently and indicates a package count of 30 tablets. Manufactured by Camber Pharmaceuticals, Inc. with contact details and storage instructions included. Also notes manufacturing by Hetero Labs Limited, Hyderabad, India.*
FDA Label Image

Fenofibrate48mgcarton (Fenofibrate48mgcarton)

Fenofibrate48mgcarton (Fenofibrate48mgcarton)
Packaging label for Fenofibrate Tablets, USP 48 mg, film-coated tablets by Camber Pharmaceuticals, Inc. The label shows the NDC 31722-595-32, indicates 100 (10 x 10) unit dose tablets, and states Rx only. Manufacturer information includes Hetero Labs Limited, India, and Camber Pharmaceuticals in Piscataway, NJ. The label includes storage instructions and notes the package is not child-resistant.*
FDA Label Image

Fenofibrate48mgfoil (Fenofibrate48mgfoil)

Fenofibrate48mgfoil (Fenofibrate48mgfoil)
Fenofibrate Tablet USP 48 mg film-coated tablets label showing multiple identical circular labels. Each label includes the product name, strength, a barcode, and a warning to protect from moisture. Manufactured for Camber Pharmaceuticals, Inc. by HETERO LABS LIMITED, with the HETERO trademark noted.*
FDA Label Image

Fenofibrateaddress1 (Fenofibrateaddress1)

FDA Label Image

Fenofibratestructure (Fenofibratestructure)

Fenofibratestructure (Fenofibratestructure)
Chemical structure of fenofibrate, showing its molecular arrangement with labeled atoms including chlorine and various carbon groups. This diagram represents the active ingredient fenofibrate used in the prescription drug tablets by Camber Pharmaceuticals, Inc.*

* 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.