Selegiline Hydrochloride Capsule
Product Images NDC 71335-2676

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 71335-2676). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Structure (Structure)

Structure (Structure)
Chemical structure of Selegiline Hydrochloride showing its molecular arrangement including a phenyl group, alkyne side chain, and hydrochloride component.*
FDA Label Image

Table (Table)

Table (Table)
A data table presenting the incidence of treatment-emergent adverse experiences in a placebo-controlled clinical trial. It lists various adverse events and the number of patients reporting each event in two groups: selegiline hydrochloride (N=49) and placebo (N=50). Events include nausea, dizziness, abdominal pain, confusion, hallucinations, dry mouth, vivid dreams, dyskinesias, headache, and several others reported once in either or both groups.*
FDA Label Image

Label (Lbl713352676)

Label (Lbl713352676)
Label for Selegiline Hydrochloride Capsules USP 5 mg, showing a package containing 30 capsules. The label includes the NDC number 71335-2676-1, manufacturer Novitium Pharma LLC, and repackager Bryant Ranch Prepack, Inc., Burbank CA. Storage instructions and usage warnings are also printed, along with QR codes for additional information.*

* 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.