Sodium Phenylbutyrate Tablet
Product Images NDC 49884-170

3 FDA label images from Par Health Usa, Llc · 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 Sodium Phenylbutyrate (NDC 49884-170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Par Health Usa, Llc, 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

Sodium-phenyl (Sodium Phenylbutyrate Tablets 1)

Sodium-phenyl (Sodium Phenylbutyrate Tablets 1)
Chemical structure diagram of Sodium Phenylbutyrate, showing a benzene ring attached to a butyrate chain with a sodium ion.*
FDA Label Image

Sodium Phenylbutyrate Tablet (Sodium Phenylbutyrate Tablets 2)

Sodium Phenylbutyrate Tablet (Sodium Phenylbutyrate Tablets 2)
Label for Sodium Phenylbutyrate Tablets 500 mg, an oral prescription drug by Par Health USA, LLC. The label states each tablet contains 500 mg of Sodium Phenylbutyrate and the package contains 250 tablets. It includes storage instructions, dispensing advice for pharmacists, and a barcode. The product NDC is 49884-170-04.*
FDA Label Image

Sodium Phenylbutyrate Tablet (Sodium Phenylbutyrate Tablets 3)

Sodium Phenylbutyrate Tablet (Sodium Phenylbutyrate Tablets 3)
Box label for Sodium Phenylbutyrate Tablets 500 mg by Par Pharmaceutical. The prescription oral tablet package contains 250 tablets. The label includes dosage and storage guidance, manufacturer information, and a barcode, with clear branding and NDC 49884-170.*

* 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.