Deflazacort Tablet
Product Images NDC 70095-042

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Deflazacort (NDC 70095-042). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

18mg-bottle (18mg Bottle)

Deflazacort Tablets 18 mg oral tablets label from Sun Pharmaceutical Industries, Inc. The label states the quantity as 30 tablets, for prescription use only, and includes storage instructions and manufacturer information. A barcode and NDC 70095-041-30 are also visible.*

FDA Label Image

18mg-carton (18mg Carton)

Deflazacort Tablets 18 mg oral tablets packaging label with a quantity of 30 tablets. Label states Rx only and includes storage instructions to keep out of reach of children and store between 20°C to 25°C, with excursions permitted between 15°C to 30°C. Manufactured by Ohm Laboratories Inc. and distributed by Sun Pharmaceutical Industries, Inc. Contains multiple barcodes and the Sun Pharma logo.*

FDA Label Image

30mg-bottle (30mg Bottle)

Label for Deflazacort Tablets 30 mg oral tablets, manufactured by Ohm Laboratories Inc. and distributed by Sun Pharmaceutical Industries, Inc. The package contains 30 tablets. The label includes storage instructions, dosage and administration notes, and a barcode. The right end of the label indicates a non-vanish area.*

FDA Label Image

30mg-carton (30mg Carton)

Packaging label for Deflazacort Tablets 30 mg, distributed by Sun Pharmaceutical Industries, Inc. The label states the product is for oral use, Rx only, and contains 30 tablets. Storage instructions and dosage advisories are included, along with manufacturer information (Ohm Laboratories Inc., New Brunswick, NJ). Multiple barcodes and the Sun Pharma logo are visible on the flattened box layout.*

FDA Label Image

36mg-bottle (36mg Bottle)

Label for Deflazacort Tablets 36 mg oral tablets by Sun Pharmaceutical Industries, Inc. The label indicates a package of 30 tablets, Rx only, with storage instructions and manufacturer details. The label includes a barcode and states the product is for oral use.*

FDA Label Image

36mg-carton (36mg Carton)

Packaging label for Deflazacort Tablets 36 mg for oral use. The label indicates the product contains 30 tablets and is manufactured by Ohm Laboratories, Inc. and distributed by Sun Pharmaceutical Industries, Inc. It includes dosage and storage instructions, NDC 70095-043-30, and features barcodes and the Sun Pharma logo.*

FDA Label Image

6mg-bottle (6mg Bottle)

Deflazacort 6 mg tablets for oral use by Sun Pharmaceutical Industries, Inc. The label indicates a package of 100 tablets, Rx only. It includes dosage strength prominently in a purple bar, a barcode, manufacturing and distribution information, and storage instructions.*

FDA Label Image

6mg-carton (6mg Carton)

Label for Deflazacort Tablets 6 mg oral tablets by Sun Pharmaceutical Industries, Inc. The label includes NDC 70095-040-01 and states a package size of 100 tablets. It features storage instructions, dosage administration directions to see package insert, and warnings to keep out of reach of children. Manufactured by Ohm Laboratories Inc., New Brunswick, NJ.*

FDA Label Image

Defla-structure (Defla Structure)

Chemical structure of the active ingredient Deflazacort, a corticosteroid represented by a multi-ring molecular structure with hydroxyl (OH), acetoxy (AcO), and ketone groups.*

* 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.