Formula (Oxycodone Hydrochloride Tablets Usp 1)
Oxycodone Hydrochloride Tablet
Product Images NDC 65162-050
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Oxycodone Hydrochloride (NDC 65162-050). 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.
Product Images & Figures Index
Oxycodone Hydrochloride Tablets Usp 10
Not available. The provided text does not contain a coherent description.*
Oxycodone Hydrochloride Tablets Usp 11
NDC 65162-051-03 is a pharmaceutical product consisting of tablets containing 30mg of Oxycodone Hydrochloride, USP. The usual dosage is indicated in the package insert. The product should be stored between 20°C to 25°C with protection from moisture. Dispensing requires a DEA order form in a tightly sealed container with a child-resistant closure. The medication guide should be dispensed to each patient. Manufactured by Amneal Pharmaceuticals of NY, LLC.*
Oxycodone Hydrochloride Tablets Usp 12
Figure 1 (Oxycodone Hydrochloride Tablets Usp 2)
5 mg (Oxycodone Hydrochloride Tablets Usp 3)
This is a medication description for oxycodone hydrochloride tablets, 5mg dosage. The package insert should be referred to for complete prescribing information. The tablets should be stored at room temperature, protected from moisture, and dispensed in a tightly sealed and child-resistant container. A medication guide should be provided to each patient, and a DEA order form is required for a 30 tablet prescription. Manufactured by Amneal Pharmaceuticals of NY, LLC. There is no specific indication or product name mentioned.*
10 mg (Oxycodone Hydrochloride Tablets Usp 4)
15 mg (Oxycodone Hydrochloride Tablets Usp 5)
NDC 65162-048-03 is a medication guide for Oxycodone Hydrochloride Tablets, USP. Each tablet contains 10 mg of oxycodone hydrochloride, USP. It is recommended to dispense the medication guide to each patient. The usual dosage can be found in the package insert. The tablets should be stored between 20° to 25°C and protected from moisture. It is required to dispense the medication in a tight, light-resistant container with a child-resistant closure. The manufacturer is Amneal Pharmaceuticals of NY, LLC located in Brookhaven, NY. DEA order form is required.*
20 mg (Oxycodone Hydrochloride Tablets Usp 6)
30 mg (Oxycodone Hydrochloride Tablets Usp 7)
This is the description of a medication labeled as NDC 65162-049-03. Each tablet contains 15MG of oxycodone hydrochloride, USP. The usual dosage should be reviewed by referring to the package insert for complete prescribing information. This medication should be stored between 20°C to 25°C (68°F to 77°F), with excursions permitted between 15°C to 30°C (59°F to 86°F) but should be protected from moisture. It should be dispensed in a tight, light-resistant container as defined in the USP, with a child-resistant closure. Each patient should be given a medication guide accompanied by DEA order form required. The medication is manufactured by Amneal Pharmaceuticals of NY, LLC, located in Brookhaven, NY 11719.*
Oxycodone Hydrochloride Tablets Usp 8
Oxycodone Hydrochloride Tablets Usp 9
NDC 65162-050-03 is a package of Oxycodone Hydrochloride tablets, USP containing 20mg of oxycodone in each tablet. The medication guide should be given to each patient. The proper dosage and other prescribing information can be found in the package insert. The tablets should be stored at temperatures between 20-25°C and protected from moisture. A DEA order form is required to dispense. The manufacturer is Amneal Pharmaceuticals of NY, LLC in Brookhaven, NY.*
* 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.
