Oxycodone Hydrochloride Tablet
Product Images NDC 67296-2233

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 67296-2233). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Formula (Oxycodone Hydrochloride Tablets Usp 1)

Formula (Oxycodone Hydrochloride Tablets Usp 1)
Chemical structure of oxycodone hydrochloride depicted with labeled molecular components, including carbon, hydrogen, oxygen, nitrogen atoms, and associated hydrochloride (HCl). Molecular formula is indicated as C18H21NO4 plus HCl, with a molecular weight of approximately 351.82.*
FDA Label Image

4 (Oxycodone Hydrochloride Tablets Usp 10)

4 (Oxycodone Hydrochloride Tablets Usp 10)
Oxycodone Hydrochloride Tablets, USP 20 mg oral tablets packaging label showing quantity of 100 tablets by Amneal. Label includes NDC 65162-050-10, controlled substance schedule II symbol, storage instructions, manufacturer details for Amneal Pharmaceuticals of NY, LLC, and a pharmacist dispensing note. Barcode and QR code for medication guide are present.*
FDA Label Image

5 (Oxycodone Hydrochloride Tablets Usp 11)

5 (Oxycodone Hydrochloride Tablets Usp 11)
Oxycodone Hydrochloride Tablets USP 30 mg label from Amneal Pharmaceuticals of NY, LLC. The label shows the dosage strength, NDC 65162-051-03, and contains 30 tablets. It includes storage instructions, DEA order form note, and dispensing guidance, with a green and white color scheme and the Amneal logo.*
FDA Label Image

5 (Oxycodone Hydrochloride Tablets Usp 12)

5 (Oxycodone Hydrochloride Tablets Usp 12)
Label for Oxycodone Hydrochloride Tablets USP 30 mg, oral tablets in a package of 100 tablets. The label includes the NDC 65162-051-10, states the product is Rx only, and features the Amneal logo. The label provides storage instructions and a QR code linking to the medication guide. It is manufactured by Amneal Pharmaceuticals of NY, LLC.*
FDA Label Image

Figure 1 (Oxycodone Hydrochloride Tablets Usp 2)

Figure 1 (Oxycodone Hydrochloride Tablets Usp 2)
A pharmacokinetic concentration-time curve showing plasma concentration over 25 hours for Oxycodone 5 mg tablets administered in quantities of 1, 3, and 6. The graph illustrates how concentration peaks and declines over time for each tablet count, labeled respectively.*
FDA Label Image

1 (Oxycodone Hydrochloride Tablets Usp 3)

1 (Oxycodone Hydrochloride Tablets Usp 3)
Label for Oxycodone Hydrochloride Tablets, USP 5 mg, oral dosage form. The label shows the product name, strength (5 mg), and quantity (30 tablets). It is marked Rx only and includes storage instructions and manufacturer information: Amneal Pharmaceuticals of NY, LLC. The label also notes that it is a Schedule II controlled substance, with a DEA order form required.*
FDA Label Image

1 (Oxycodone Hydrochloride Tablets Usp 4)

1 (Oxycodone Hydrochloride Tablets Usp 4)
Label for Oxycodone Hydrochloride Tablets, USP 5 mg, oral tablet in 100 count packaging by Amneal Pharmaceuticals. The label shows dosage strength, drug name, NDC 65162-047-10, storage instructions, and manufacturer details (Amneal Pharmaceuticals of NY, LLC). It includes a QR code to the medication guide and a DEA order form notice.*
FDA Label Image

2 (Oxycodone Hydrochloride Tablets Usp 5)

2 (Oxycodone Hydrochloride Tablets Usp 5)
Label for Oxycodone Hydrochloride Tablets, USP 10 mg showing proprietary name, strength, and dosage form. The label includes a depiction of a purple tablet, states 'Rx only,' and indicates a package size of 30 tablets. The labeler is Amneal Pharmaceuticals of NY, LLC, with storage and dispensing instructions, a DEA order form requirement, and a barcode.*
FDA Label Image

2 (Oxycodone Hydrochloride Tablets Usp 6)

2 (Oxycodone Hydrochloride Tablets Usp 6)
Oxycodone Hydrochloride Tablets, USP 10 mg oral tablets packaging label from Amneal Pharmaceuticals. The label shows a bottle of 100 tablets with a purple round tablet imprinted "A 48". It includes directions for pharmacists, storage instructions, DEA order requirement statement, and manufacturer information. The NDC code on the label is 65162-048-10.*
FDA Label Image

3 (Oxycodone Hydrochloride Tablets Usp 7)

3 (Oxycodone Hydrochloride Tablets Usp 7)
Label for Oxycodone Hydrochloride Tablets, USP 15 mg, produced by Amneal Pharmaceuticals of NY, LLC. The label includes dosage strength, quantity of 30 tablets, controlled substance classification, storage instructions, and a barcode. It also notes the product requires a DEA order form and is designated Rx only.*
FDA Label Image

3 (Oxycodone Hydrochloride Tablets Usp 8)

3 (Oxycodone Hydrochloride Tablets Usp 8)
Oxycodone Hydrochloride Tablets USP 15 mg oral tablet label, showing a single green tablet image. The label includes dosage strength (15 mg), quantity (100 tablets), and pharmacological classification (Schedule II). Labeler is Amneal Pharmaceuticals of NY, LLC. Additional information includes storage instructions, a QR code for medication guide, and dispensing notes. NDC 65162-049-10.*
FDA Label Image

4 (Oxycodone Hydrochloride Tablets Usp 9)

4 (Oxycodone Hydrochloride Tablets Usp 9)
Label for Oxycodone Hydrochloride Tablets, USP 20 mg, oral tablet, showing product name and strength prominently. The label includes the NDC 65162-050-03 and states it is a Schedule II controlled substance. Manufacturer is Amneal Pharmaceuticals of NY, LLC. The package contains 30 tablets. Storage instructions, dosage directions to consult the insert, and a barcode are also visible.*

* 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.