Amikacin Sulfate Injection, Solution
Product Images NDC 23155-290

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Amikacin Sulfate (NDC 23155-290). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Heritage Pharmaceuticals Inc. D/b/a Avet 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

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Chemical structure of Amikacin Sulfate as depicted in the image, showing the molecular arrangement including sulfate ions.*

FDA Label Image

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FDA Label Image

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Label for Amikacin Sulfate Injection, USP, 500 mg/2 mL (250 mg/mL) single-dose vial. The label indicates use for intramuscular or intravenous administration. It includes storage instructions, manufacturer Emcure Pharmaceuticals Ltd., and marketing by Avet Pharmaceuticals Inc. The label features a barcode and revision date of 12/2020.*

FDA Label Image

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Amikacin Sulfate Injection, USP 500 mg/2 mL (250 mg/mL) solution for injection, for intramuscular or intravenous use. Pack contains 10 single-dose 2 mL vials. Labeler is Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. NDC 23155-290. The label includes storage and dosage information and manufacturer details.*

FDA Label Image

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Label for Amikacin Sulfate Injection, USP 1 gram/4 mL (250 mg/mL) solution for injection. The single-dose vial contains 4 mL and is indicated for intramuscular or intravenous use. The label notes the product is equivalent to Amikacin and is distributed by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.*

FDA Label Image

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The packaging label for Amikacin Sulfate Injection, USP 1 gram/4 mL (250 mg/mL) by Avet Pharmaceuticals Inc. It is a solution for injection, for intramuscular or intravenous use, supplied in 10 single-dose vials of 4 mL each. The label includes the NDC 23155-290, manufacturer information, and dosage details.*

* 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.