Trientine Hydrochloride Capsule
Product Images NDC 16571-810

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Trientine Hydrochloride (NDC 16571-810). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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

Trientine-hcl-250.jpg (Trientine HCl 250)

Label for Trientine Hydrochloride Capsules, USP 250 mg by Rising Pharma Holdings, Inc. The label states the product contains 100 capsules and is for prescription use only. It includes storage instructions, dispensing guidelines, manufacturer address, and a barcode.*

FDA Label Image

Trientine-hcl-250-carton.jpg (Trientine HCl 250 Carton)

Packaging label for Trientine Hydrochloride Capsules, USP 250 mg, by Rising Pharma Holdings, Inc. The box design includes the proprietary name, dosage strength, quantity of 100 capsules, and directions to dispense only in the original container. The label also features a barcode, storage instructions, and the Rx only designation.*

FDA Label Image

Trientine-hcl-500.jpg (Trientine HCl 500)

Label for Trientine Hydrochloride Capsules, USP 500 mg, in a 50-capsule package. The product is labeled by Rising Pharmaceuticals and indicates dispensing only in the original container. It includes storage instructions to keep below 25°C, and it notes it is manufactured for Rising Pharma Holdings, Inc. in East Brunswick, NJ, with manufacturing in India.*

FDA Label Image

Trientine-hcl-500-carton.jpg (Trientine HCl 500 Carton)

Box packaging label for Trientine Hydrochloride Capsules, USP 500 mg by Rising Pharma Holdings, Inc. The label shows the product name, strength, dosage form as capsules, route oral, quantity 50 capsules, and notes Rx only. The label includes manufacturer information, barcode, NDC 16571-812-05, and storage instructions to keep below 25°C (77°F).*

* 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.