Dronabinol Structural Formula (Syndros 01)
Syndros
Product Images NDC 20482-335
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Syndros (NDC 20482-335). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Insys Therapeutics, 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.
Product Images & Figures Index
Figure A (Syndros 02)
The text seems to be a product description for a medication dispenser. It includes a white child-resistant plunger with a ring and barrel. It also includes an adapter for an oral syringe. The product appears to be called Syndros and features a ribbed X-eng plunger. Figure A may be a diagram or illustration of the product.*
Figure B (Syndros 03)
Figure C (Syndros 04)
Figure D (Syndros 05)
Figure E (Syndros 06)
Figure F (Syndros 07)
Figure G (Syndros 08)
Figure H (Syndros 09)
Figure I (Syndros 10)
Figure J (Syndros 11)
Figure K (Syndros 12)
Figure L (Syndros 13)
Figure M (Syndros 14)
30 mL Bottle Label (Syndros 15)
This text is a product label for Syndros containing important information about its contents and usage. It includes the manufacturer's name, dosage information, storage instructions, and contact information for additional questions. The medication is an oral solution containing dronabinol, and must be refrigerated before use. However, once opened, it can be stored at room temperature. The label includes important warnings about the product and its usage.*
30 mL Carton Label (Syndros 16)
This is a description for an oral solution called Syndros® containing 5 mg dronabinol, used for oral administration only. The solution is stored between 2° and 8°C and must be refrigerated and protected from light. It comes in a 30mL light-resistant bottle with an oral syringe and adapter. The container has a tamper-evident seal; it cannot be used if broken or missing. Before use, the package insert must be consulted for full prescribing information. The unused portion must be discarded after 43 days of first opening. It is manufactured by Insys Therapeutics, Inc, in Chandler, AZ, and distributed by Renaissance Lakewood, LLC, in Lakewood, NJ. Pharmacists are advised to provide patients with dosing instructions in milliliters (mL) and round the dose to the nearest 0.1 mL increment.*
Figure N (Syndros 17)
Figure O (Syndros 18)
Figure P (Syndros 19)
* 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.
