Triamcinolone Acetonide Injection, Suspension
Product Images NDC 70121-1169

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Triamcinolone Acetonide (NDC 70121-1169). 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

Chem Structure (Triamcinolone Acetonide Injectable Suspension Usp 1)

Chem Structure (Triamcinolone Acetonide Injectable Suspension Usp 1)
Chemical structure diagram of Triamcinolone Acetonide, showing its molecular bonds and hydroxyl, fluorine, and acetate functional groups.*
FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Usp 2)

1 (Triamcinolone Acetonide Injectable Suspension Usp 2)
Label for Triamcinolone Acetonide Injectable Suspension, USP 40 mg per mL by Amneal Pharmaceuticals LLC. The label states it is for intramuscular or intra-articular use only and is Rx only. It also includes storage instructions, a barcode, and manufacturing details.*
FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Usp 3)

1 (Triamcinolone Acetonide Injectable Suspension Usp 3)
Label for Triamcinolone Acetonide Injectable Suspension, USP 40 mg per mL by Amneal Pharmaceuticals LLC. This 1 mL single-dose vial is for intramuscular or intra-articular use only. The label includes dosage form, strength, usage instructions, storage conditions, and manufacturer details, along with barcode and NDC 70121-1049-2.*
FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Usp 4)

1 (Triamcinolone Acetonide Injectable Suspension Usp 4)
Packaging label for Triamcinolone Acetonide Injectable Suspension, USP 40 mg per mL by Amneal Pharmaceuticals LLC. This label is for 25 single-dose 1 mL vials, for intramuscular or intra-articular use only. It includes storage instructions, usage warnings, and manufacturer information, with a barcode and Amneal logo.*
FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Usp 5)

1 (Triamcinolone Acetonide Injectable Suspension Usp 5)
Triamcinolone Acetonide Injectable Suspension, USP 200 mg per 5 mL (40 mg per mL) in a 5 mL multiple-dose vial label. The product is for intramuscular or intra-articular use only and is Rx only. Labeler is Amneal Pharmaceuticals LLC, with manufacturing and packaging information included.*
FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Usp 6)

1 (Triamcinolone Acetonide Injectable Suspension Usp 6)
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. It includes storage instructions, usage warnings, manufacturer and distributor information, and a barcode.*
FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Usp 7)

1 (Triamcinolone Acetonide Injectable Suspension Usp 7)
Triamcinolone Acetonide Injectable Suspension USP, 400 mg per 10 mL (40 mg per mL), for intramuscular or intra-articular use only. The label indicates a 10 mL multiple-dose vial, RX only, labeled by Amneal Pharmaceuticals LLC, with a barcode and storage instructions.*
FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Usp 8)

1 (Triamcinolone Acetonide Injectable Suspension Usp 8)
Packaging label for Triamcinolone Acetonide Injectable Suspension, USP 400 mg per 10 mL (40 mg per mL) by Amneal Pharmaceuticals LLC. The label indicates it is for intramuscular or intra-articular use only and comes in a 10 mL multiple-dose vial. It includes storage instructions, warnings, and manufacturer information.*

* 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.