Selegiline Hydrochloride Capsule
Product Images NDC 16571-659

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Selegiline Hydrochloride (NDC 16571-659). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

500ct

500ct
This appears to be a label of medication called Selegiline Hydrochloride, which comes in a bottle with 500 capsules. The manufacturer could be "Rising" and the product may comply with the United States Pharmacopeia.*
FDA Label Image

60ct

FDA Label Image

Chemical Structure (Chemstructure)

FDA Label Image

Adverse Reactions Table (Table Adverse Events V2)

Adverse Reactions Table (Table Adverse Events V2)
This text provides a table that shows the incidence of adverse events in a clinical trial that was placebo-controlled. The trial evaluated the effect of selegiline hydrochloride in a group of 50 patients versus placebo in a group of 49 patients. The table shows the number of patients reporting each adverse event. The adverse events reported in the selegiline hydrochloride group include nausea, dizziness/light-headed/fainting, abdominal pain, confusion, hallucinations, dry mouth, dyskinesias, headache, and vivid dreams. The placebo group reported aches, anxiety/tension, anemia, diarrhea, hair loss, insomnia, leg pain, low back pain, malaise, palpitations, urinary retention, lethargy, and weight loss.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.