Prednisone Tablet
Product Images NDC 60219-1707

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Prednisone (NDC 60219-1707). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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.

FDA Label Image

Structure (Prednisone Tablets Usp 10 mg And 20 mg 1)

Structure (Prednisone Tablets Usp 10 mg And 20 mg 1)
Chemical structure diagram of prednisone, a corticosteroid medication. The diagram shows its molecular framework including rings and functional groups typical to prednisone's chemical composition.*
FDA Label Image

10 (Prednisone Tablets Usp 10 mg And 20 mg 2)

10 (Prednisone Tablets Usp 10 mg And 20 mg 2)
The label is for prednisone tablets, USP, 10 mg strength, under the brand name predniSONE by Amneal Pharmaceuticals NY LLC. It indicates the package contains 100 tablets. The label includes dosage information, storage instructions (store at 20° to 25°C, protect from moisture), and manufacturing details showing Amneal Pharmaceuticals Pvt. Ltd. in Ahmedabad, India, and distribution by Amneal Pharmaceuticals LLC in Bridgewater, NJ. The label also has a barcode and a depiction of the tablet marked with 'A 19'.*
FDA Label Image

1 (Prednisone Tablets Usp 10 mg And 20 mg 3)

1 (Prednisone Tablets Usp 10 mg And 20 mg 3)
Label for prednisone 10 mg oral tablets, USP, showing 500 tablets in the package. Manufactured by Amneal Pharmaceuticals Pvt. Ltd., distributed by Amneal Pharmaceuticals LLC. The label includes dosage form, strength, storage conditions, and a barcode, along with an image of a round tablet imprinted with 'A 48'.*
FDA Label Image

10 (Prednisone Tablets Usp 10 mg And 20 mg 4)

10 (Prednisone Tablets Usp 10 mg And 20 mg 4)
Prednisone Tablet USP 10 mg oral tablets label strips from Amneal Pharmaceuticals NY LLC. Labels display the product name, strength (10 mg), barcode, directions to tear and peel the paper, and information that the product is made in India and distributed by Amneal Pharmaceuticals LLC. Each label includes placeholders for lot number and expiration date.*
FDA Label Image

10 (Prednisone Tablets Usp 10 mg And 20 mg 5)

10 (Prednisone Tablets Usp 10 mg And 20 mg 5)
Prednisone Tablets USP 10 mg unit-dose packaging label by Amneal Pharmaceuticals NY LLC. The label includes dosage strength in orange, branding with predniSONE highlighted, and states 100 (10 x 10) unit-dose tablets per package. Storage instructions and manufacturer details are provided, along with a barcode and NDC 60219-1707-3.*
FDA Label Image

10 (Prednisone Tablets Usp 10 mg And 20 mg 6)

10 (Prednisone Tablets Usp 10 mg And 20 mg 6)
Label for prednisone tablets USP, 20 mg, by Amneal Pharmaceuticals NY LLC. The label includes the NDC number 60219-1708-1, a single round tablet imprinted with AC 72 at actual size, and states the product is a prescription oral solid dosage. The package contains 100 tablets and provides storage instructions and manufacturer details.*
FDA Label Image

10 (Prednisone Tablets Usp 10 mg And 20 mg 7)

10 (Prednisone Tablets Usp 10 mg And 20 mg 7)
Label for prednisone Tablets, USP 20 mg oral tablets by Amneal Pharmaceuticals NY LLC. The label shows the product name with 20 mg strength, 500 tablets count, and includes an image of a round tablet marked with AC 72. Storage instructions and manufacturer details (Amneal Pharmaceuticals Pvt. Ltd., India) are also provided.*

* 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.