Paroxetine
Product Images NDC 58118-0184

3 FDA label images from Clinical Solutions Wholesale, 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 Paroxetine (NDC 58118-0184). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Clinical Solutions Wholesale, 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.

Product Images & Figures Index

FDA Label Image

Paroxetine 30mg Tablet 30 Count Bister Card (Image 02)

Paroxetine 30mg Tablet 30 Count Bister Card (Image 02)
Packaging label for Paroxetine 30 mg tablets by Clinical Solutions Wholesale, manufactured by Zydus Pharmaceuticals (USA). The label includes the NDC 58118-0184-8, manufacturing NDC and lot number, batch number, expiration date of September 2018, quantity of 30 tablets, and packaging details for repackaging and distribution.*
FDA Label Image

Paroxetine 20mg

Paroxetine 20mg
Label for Paroxetine 20mg tablets from Clinical Solutions Wholesale, LLC. The label displays the product name, strength, dosage form, NDC number 58118-0183-8, quantity of 30 tablets, manufacturing details including Mfg. NDC 68382-0098-16, lot number SAMPLE123, and expiration date September 2021. The manufacturer is Ives Pharmaceuticals (USA) located in Pennington, NJ.*
FDA Label Image

Structured Formula For Paroxetine (Paroxetine Figure 01)

Structured Formula For Paroxetine (Paroxetine Figure 01)
Chemical structure diagram of Paroxetine hydrochloride, showing its molecular configuration with labeled atoms and bonds, including fluorophenyl and methylenedioxy 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.