Selegiline Hydrochloride Capsule
Product Images NDC 70954-504

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Selegiline Hydrochloride (NDC 70954-504). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novitium Pharma 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.

FDA Label Image

Structure (Structure)

Chemical structure of Selegiline Hydrochloride, showing its molecular arrangement including the phenyl group, alkyne side chain, and hydrochloride component.*

FDA Label Image

Table (Table)

A table showing the incidence of treatment-emergent adverse experiences in a placebo-controlled clinical trial for Selegiline Hydrochloride. It lists adverse events such as nausea, dizziness, abdominal pain, confusion, hallucinations, dry mouth, vivid dreams, dyskinesias, and headache, with the number of patients reporting each event for both the selegiline hydrochloride group (N=49) and the placebo group (N=50). Additional events reported once in either or both groups are also detailed.*

FDA Label Image

Label-1000ct (Label 1000ct)

Label for Selegiline Hydrochloride Capsules, USP 5 mg, oral capsules. The package contains 1000 capsules and is labeled by Novitium Pharma LLC. It includes storage instructions, dosage information, a barcode, and notes that the product is Rx only.*

FDA Label Image

Label-60ct (Label 60ct)

Label for Selegiline Hydrochloride Capsules, USP, 5 mg strength, containing 60 capsules per bottle. The label shows the NDC 70954-504-10, manufactured by Novitium Pharma LLC, with storage and dispensing instructions. The label includes a barcode and notes that the product is prescription only (Rx).*

* 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.