Cyproheptadine Hydrochloride Tablet
Product Images NDC 16571-805

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Cyproheptadine Hydrochloride (NDC 16571-805). 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

Cyproheptadine-1000ct.jpg (Cyproheptadine 1000ct)

Packaging label for Cyproheptadine Hydrochloride Tablets USP, 4 mg oral tablets. The label shows the product name, strength, and quantity of 1000 tablets. It includes storage instructions, dosing information reference, and a warning to keep out of reach of children. The labeler is Rising Pharma Holdings, Inc., located in East Brunswick, NJ. The label also displays the NDC 16571-805-10 and a barcode.*

FDA Label Image

Cyproheptadine-100ct.jpg (Cyproheptadine 100ct)

Label for Cyproheptadine Hydrochloride Tablets USP 4 mg by Rising Pharma Holdings, Inc. The label indicates 100 tablets, oral route, and prescription only. It includes dosing instructions referencing package insert, storage conditions between 20°C to 25°C, and a warning to keep out of reach of children. The NDC code 16571-805-01 is present, along with distribution information from East Brunswick, NJ.*

FDA Label Image

Structure.jpg (Structure)

Chemical structure diagram of Cyproheptadine Hydrochloride, showing its molecular arrangement including a tricyclic ring system and a piperidine ring with a methyl group, along with the hydrochloride component.*

* 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.