Sertraline Hydrochloride
Product Images NDC 10135-694

View Photos of 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 Sertraline Hydrochloride (NDC 10135-694). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex 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

Structural Formula (Sertraline Hydrochloride Oral Solution Usp 01)

Structural Formula (Sertraline Hydrochloride Oral Solution Usp 01)
Chemical structure of Sertraline Hydrochloride, showing a characteristic bicyclic structure with a dimethylamino group and two chlorine atoms attached to a phenyl ring.*
FDA Label Image

Sertralinehydrochlorideoral Solution Usp20 mg/ml*ndc 10135-0694-61rx Only (Sertraline Hydrochloride Oral Solution Usp 02)

Sertralinehydrochlorideoral Solution Usp20 mg/ml*ndc 10135-0694-61rx Only (Sertraline Hydrochloride Oral Solution Usp 02)
Label for Sertraline Hydrochloride Oral Solution USP by Marlex Pharmaceuticals Inc, in a 60 mL bottle. The concentration is 20 mg/mL. The label includes instructions such as dilution before use, pharmacist advice, and storage conditions. The product is Rx Only.*
FDA Label Image

Sertralinehydrochlorideoral Solution Usp20 mg/ml*ndc 10135-0694-61rx Only (Sertraline Hydrochloride Oral Solution Usp 03)

Sertralinehydrochlorideoral Solution Usp20 mg/ml*ndc 10135-0694-61rx Only (Sertraline Hydrochloride Oral Solution Usp 03)
Packaging label for Sertraline Hydrochloride Oral Solution USP, 20 mg/mL, by Marlex Pharmaceuticals Inc. The label indicates the product is a 60 mL oral solution requiring dilution before use, with a warning to always dispense with a medication guide and calibrated dropper enclosed. It notes the product is Rx only and includes NDC 10135-0694-61.*

* 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.