Triamcinolone Acetonide Injection, Suspension
Product Images NDC 0703-0245

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Triamcinolone Acetonide (NDC 0703-0245). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Parenteral Medicines, 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

Structural Formula (Image 1)

FDA Label Image

1 (Image 2)

FDA Label Image

1 (Image 3)

Triamcinolone Acetonide Injectable Suspension USP is a medication used for intramuscular or intra-articular use only. Each 5 mL multiple-dose vial provides 200 mg of Triamcinolone Acetonide at a concentration of 40 mg per mL. The medication comes with a serialization flap and should be stored in a cool and dry place. The suspension contains sodium hyaluronate as a viscous agent and carboxymethylcellulose as a suspending agent. It is manufactured in Zagred, Croatia, by Pivainatsa. Dosage instructions are available on request.*

FDA Label Image

1 (Image 4)

This is a description of a medication product. It is for a treatment that contains Triamcinolone Acetonide and Beclomethasone Dipropionate, and is manufactured in a 10 mL Multiple-Dose Vial. The medication is an Injectable Suspension USP, intended for intramuscular or intra-articular use only and comes with dosage information. The medication provides 40 mg tiamcinlone Streal and 0565% sodum chorde USP. The product is manufactured by Teva Pharmaceuticals USA, located in Horh Wales, PA.*

* 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.