Acetaminophen And Codeine Phosphate
Product Images NDC 50383-079

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Acetaminophen And Codeine Phosphate (NDC 50383-079). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akorn, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

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Chemical Structure (Image 01)

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Chemical Structure 2 (Image 02)

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Controlled Substance Symbol (Image 03)

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Bars (Image 04)

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Container Label (Image 05)

OAKORN is an oral solution that contains Acetaminophen and Codeine Phosphate. It is a prescription drug that comes in 16floz bulk container. It is important to dispense the accompanying Medication Guide to the patient. The recommended dosage for adults is 5 mL (1 tablespoonful) every four hours. OAKORN is not for household use as it may be habit-forming. The drug contains propylene glycol, purified water, saccharin sodium, Sodium benzoate, and sucrose along with its active ingredients. The drug should be stored at 15°C to 30°C and should be protected from light. The cap of the container comes with a printed safety seal around the neck that should not be accepted if broken or missing.*

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5ml (Image 06)

Delivers 5mL Acetaminophen and Codeine Phosphate Oral Solution, USP, with 7% alcohol content. This product is manufactured by HiTech Pharmacal Co, Inc. and is meant for institutional use only. It is important to protect it from light and avoid refrigeration. The NDC number for this product is 50383-337-05 and it should be stored at a temperature between 15°C to 30°C (59°F to 86°F). The label indicates that this product is manufactured in Amityville, NY 11701.*

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10ml (Image 07)

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12.5ml (Image 08)

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15ml (Image 09)

* 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.