Triamcinolone Acetonide Injection, Suspension
Product Images NDC 70121-1657

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Triamcinolone Acetonide (NDC 70121-1657). 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 Ppr 1)

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1 (Triamcinolone Acetonide Injectable Suspension Ppr 2)

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1 (Triamcinolone Acetonide Injectable Suspension Ppr 3)

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2 (Triamcinolone Acetonide Injectable Suspension Ppr 4)

This is a description for a medication called "Triamcinolone Acetonide Injectable Suspension, USP". It is a 1 mL single-dose vial for intramuscular or intra-articular use only. The medication is manufactured by "Amneal Pharmaceuticals Pvt Ltd" and distributed by "Amneal Pharmaceuticals LLC". The product has an NDC (National Drug Code) number of 70121-1657-1. The label warns that unused portions must be discarded and that it should be used with caution. The text provides storage instructions and lists some precautions.*

FDA Label Image

25 (Triamcinolone Acetonide Injectable Suspension Ppr 5)

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1 (Triamcinolone Acetonide Injectable Suspension Ppr 6)

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2 (Triamcinolone Acetonide Injectable Suspension Ppr 7)

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1 (Triamcinolone Acetonide Injectable Suspension Ppr 8)

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2 (Triamcinolone Acetonide Injectable Suspension Ppr 9)

This is a pharmaceutical label for Triamcinolone Acetonide Injectable Suspension, USP with 400 mg per 10mL. It is intended for intramuscular or intraarticular use only and is available in a 10mL multiple dose vial. The label also contains directions and warnings on proper usage and storage.*

* 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.