Opium Tincture Deodorized Solution
Product Images NDC 62559-153

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Opium Tincture Deodorized (NDC 62559-153). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ani Pharmaceuticals, 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

Label.jpg (Label)

This is a prescription medication containing anhydrous morphine and alcohol. Each 100 mL of the medication contains 1 g of anhydrous morphine which is equivalent to 10 g of Powdered Opium USP. The alcohol concentration is 19%. The medication should be kept out of reach of children and stored at controlled room temperature. The recommended dosage for an adult is 0.6 mL orally 4 times a day. The medication comes in a 118 mL (4 1.oz.) container and should be dispensed in a tight, light-resistant container as defined in the USP. Full prescribing information for Tincture USP is included in an attached insert. This medication is manufactured by ANI Pharmaceuticals, Inc. in Baudette, MN 56623.*

FDA Label Image

Ani (Ani Logo)

* 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.