Selegiline Hydrochloride Capsule
Product Images NDC 10135-737

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 Selegiline Hydrochloride (NDC 10135-737). 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

Struct (Structure)

Struct (Structure)
Chemical structure of Selegiline Hydrochloride depicting its molecular arrangement including a phenyl group, methyl groups, and a hydrochloride salt component.*
FDA Label Image

Table (Table)

Table (Table)
A table showing the incidence of treatment-emergent adverse experiences in a placebo-controlled clinical trial comparing selegiline hydrochloride and placebo. It lists various adverse events and the number of patients reporting each event in both the selegiline hydrochloride group (N=49) and the placebo group (N=50). Additional events reported once in either or both groups are also included.*
FDA Label Image

Label (Label 60ct)

Label (Label 60ct)
Selegiline Hydrochloride Capsules, USP 5 mg by Marlex Pharmaceuticals, Inc. The label indicates 60 capsules per bottle with dosage form as oral capsules, Rx only. Additional label details include storage instructions at 20° to 25°C, dispensing in a tight, light-resistant container, and typical adult dosage of two capsules daily. The label also features the NDC 10135-737 and contact information for Marlex Pharmaceuticals in New Castle, DE.*

* 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.