Triamcinolone Acetonide Injection, Suspension
Product Images NDC 70121-1653

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Triamcinolone Acetonide (NDC 70121-1653). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

1 (Triamcinolone Acetonide Injectable Suspension Nova 1)

Chemical structure of Triamcinolone Acetonide, a corticosteroid active ingredient with a molecular weight of 434.50.*

FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Nova 2)

FDA Label Image

Vial (Triamcinolone Acetonide Injectable Suspension Nova 3)

Label for Triamcinolone Acetonide Injectable Suspension, USP, 40 mg per mL, for intramuscular or intra-articular use only. The label includes storage instructions, distributor Amneal Pharmaceuticals LLC, and indicates the product is made in India. It features the Novaplus logo and a barcode.*

FDA Label Image

Carton (Triamcinolone Acetonide Injectable Suspension Nova 4)

Packaging label for Triamcinolone Acetonide Injectable Suspension USP, 40 mg per mL, in a 1 mL single-dose vial. The label specifies use for intramuscular or intra-articular administration, with instructions to discard unused portions and read all sides. The labeler is Amneal Pharmaceuticals LLC, with manufacturing information also shown. The label includes storage directions and a barcode.*

FDA Label Image

Carton (Triamcinolone Acetonide Injectable Suspension Nova 5)

Packaging label for Triamcinolone Acetonide Injectable Suspension, USP, 40 mg/mL. The label indicates a 25 x 1 mL single-dose vial carton intended for intramuscular or intra-articular use only. Manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. The label includes storage instructions, usage warnings, and a barcode.*

FDA Label Image

Vial (Triamcinolone Acetonide Injectable Suspension Nova 6)

Label for Triamcinolone Acetonide Injectable Suspension USP, 200 mg per 5 mL (40 mg per mL), for intramuscular or intra-articular use only. The label includes storage and usage warnings, manufacturer Amneal Pharmaceuticals LLC, and mentions a 5 mL multiple-dose vial. The product is marked Rx only.*

FDA Label Image

Carton (Triamcinolone Acetonide Injectable Suspension Nova 7)

Packaging label for Triamcinolone Acetonide Injectable Suspension, USP 200 mg per 5 mL (40 mg per mL) by Amneal Pharmaceuticals LLC. The label indicates a 5 mL multiple-dose vial for intramuscular or intra-articular use only, with storage instructions and manufacturer details. The product is marked Rx ONLY and features the Novaplus logo.*

FDA Label Image

Vial (Triamcinolone Acetonide Injectable Suspension Nova 8)

Label of Triamcinolone Acetonide Injectable Suspension, USP, 400 mg per 10 mL (40 mg per mL) in a 10 mL multiple-dose vial by Amneal Pharmaceuticals LLC. Intended for intramuscular or intra-articular use only, this prescription drug label includes instructions to shake well and storage notes. Made in India with a red, yellow, and white color scheme featuring the 'novaplus' logo.*

FDA Label Image

Carton (Triamcinolone Acetonide Injectable Suspension Nova 9)

Triamcinolone Acetonide Injectable Suspension, USP 400 mg per 10 mL (40 mg/mL) in a 10 mL multiple-dose vial. The packaging indicates use for intramuscular or intra-articular injection only. Labeler information shows Amneal Pharmaceuticals LLC with manufacturing in India. The label includes storage instructions, dosing notes, and a barcode.*

* 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.