Triamcinolone Acetonide Injection, Suspension
Product Images NDC 70121-1655

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Triamcinolone Acetonide (NDC 70121-1655). 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)

Chemical structure of Triamcinolone Acetonide, depicting its steroid backbone with functional groups including hydroxyl, fluorine, ketone, and acetonide moieties.*

FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Ppr 2)

FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Ppr 3)

Label for Triamcinolone Acetonide Injectable Suspension, USP, 40 mg per mL, for intramuscular or intra-articular use. The label includes storage instructions to store the vial in a carton and shake well before use. The labeler is Amneal Pharmaceuticals LLC, with manufacturing in India. The label features a barcode and mentions vial size as 18 x 8 mm unit dose.*

FDA Label Image

2 (Triamcinolone Acetonide Injectable Suspension Ppr 4)

Packaging label for Triamcinolone Acetonide Injectable Suspension, USP 40 mg per mL by Amneal Pharmaceuticals LLC. The label indicates it is for intramuscular or intra-articular use only, in a 1 mL single-dose vial. It specifies storage instructions and warnings that it is not for intravenous, intradermal, intraocular, epidural, or intrathecal use.*

FDA Label Image

25 (Triamcinolone Acetonide Injectable Suspension Ppr 5)

Triamcinolone Acetonide Injectable Suspension, USP 40 mg per mL in a carton for injection suspension by Amneal Pharmaceuticals LLC. The label indicates use for intramuscular or intra-articular injection, with each carton containing 25 single-dose vials of 1 mL each. The brand PREMER ProRx is shown on the label.*

FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Ppr 6)

Label of Triamcinolone Acetonide Injectable Suspension USP, 200 mg per 5 mL (40 mg/mL) in a 5 mL multiple-dose vial by Amneal Pharmaceuticals LLC. Intended for intramuscular or intra-articular use only, with storage and usage instructions, including a barcode and manufacturer information. The label highlights the Premier ProRx brand.*

FDA Label Image

2 (Triamcinolone Acetonide Injectable Suspension Ppr 7)

Triamcinolone Acetonide Injectable Suspension, USP 200 mg per 5 mL (40 mg per mL) injection packaging label from Amneal Pharmaceuticals LLC. The product is for intramuscular or intra-articular use only, supplied in a 5 mL multiple-dose vial. The label includes storage instructions, usage warnings, and NDC codes, prominently featuring the PREMIER ProRx branding.*

FDA Label Image

1 (Triamcinolone Acetonide Injectable Suspension Ppr 8)

Label for Triamcinolone Acetonide Injectable Suspension, USP by Amneal Pharmaceuticals LLC. The product strength is 400 mg per 10 mL (40 mg per mL) in a 10 mL multiple-dose vial. Indicated for intramuscular or intra-articular use only. The label includes storage instructions and distributor information.*

FDA Label Image

2 (Triamcinolone Acetonide Injectable Suspension Ppr 9)

Triamcinolone Acetonide Injectable Suspension USP 400 mg per 10 mL (40 mg per mL) label for a 10 mL multiple-dose vial. The product is for intramuscular or intra-articular use only and is manufactured by Amneal Pharmaceuticals LLC. The label includes dosage form, strength, route of administration, storage instructions, and a recommendation to read all sides.*

* 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.