Iloperidone Tablet
Product Images NDC 0378-0632

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Iloperidone (NDC 0378-0632). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals 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

9e1900e4-eae1-4295-826c-d598e3486e5a-01 (9e1900e4 Eae1 4295 826c D598e3486e5a 01)

Chemical structure of iloperidone, showing the molecular framework of the active ingredient in ILOPERIDONE tablets, as submitted by Mylan Pharmaceuticals Inc.*

FDA Label Image

9e1900e4-eae1-4295-826c-d598e3486e5a-02 (9e1900e4 Eae1 4295 826c D598e3486e5a 02)

Label for Iloperidone 1 mg tablets by Mylan Pharmaceuticals Inc. The label indicates oral tablets with a package count of 60 tablets. Storage instructions note keeping the product at 25°C (77°F) with allowed excursions between 15° to 30°C, protecting from light and moisture. Manufacturer information includes Mylan Pharmaceuticals Inc. in the USA and Inventia Healthcare Private Limited in India. The NDC is 0378-0630-91.*

FDA Label Image

9e1900e4-eae1-4295-826c-d598e3486e5a-03 (9e1900e4 Eae1 4295 826c D598e3486e5a 03)

Label for Iloperidone 2 mg tablets, an oral human prescription drug manufactured by Mylan Pharmaceuticals Inc. The label shows 60 tablets per package, storage instructions at 25°C with permitted excursions, and warnings to protect from light and moisture. Barcode and manufacturer information for Inventia Healthcare Private Limited, India, are also visible.*

FDA Label Image

9e1900e4-eae1-4295-826c-d598e3486e5a-04 (9e1900e4 Eae1 4295 826c D598e3486e5a 04)

Label for Iloperidone 4 mg tablets by Mylan Pharmaceuticals Inc. The label includes the NDC 0378-0632-91, 60 tablets per package, and storage instructions to store at 25°C (77°F) with permitted excursions. The label also advises protection from light and moisture and keeping out of reach of children. Manufactured by Inventia Healthcare Private Limited, India.*

FDA Label Image

9e1900e4-eae1-4295-826c-d598e3486e5a-05 (9e1900e4 Eae1 4295 826c D598e3486e5a 05)

Label for Iloperidone 6 mg oral tablets by Mylan Pharmaceuticals Inc., containing 60 tablets. The label includes storage instructions, manufacturer details, a barcode, and a blue block indicating prescription use with the strength prominently displayed.*

FDA Label Image

9e1900e4-eae1-4295-826c-d598e3486e5a-06 (9e1900e4 Eae1 4295 826c D598e3486e5a 06)

Label for Iloperidone 8 mg oral tablets from Mylan Pharmaceuticals Inc. Displays one white round tablet with imprint "054". Packaging contains 60 tablets with storage instructions and manufacturer details including Inventia Healthcare Private Limited, India. NDC 0378-0634-91 noted on label.*

FDA Label Image

9e1900e4-eae1-4295-826c-d598e3486e5a-07 (9e1900e4 Eae1 4295 826c D598e3486e5a 07)

Iloperidone 10 mg tablets label showing oral prescription drug by Mylan Pharmaceuticals Inc. The label indicates 60 tablets per package, with storage instructions to keep at 25°C (77°F) and protect from light and moisture. The label also includes a barcode, manufacturer details, and a pill image marked '055'.*

FDA Label Image

9e1900e4-eae1-4295-826c-d598e3486e5a-08 (9e1900e4 Eae1 4295 826c D598e3486e5a 08)

Label for Iloperidone 12 mg tablets from Mylan Pharmaceuticals Inc. The label includes the NDC 0378-0636-91, product name, strength, and dosage form. It states the package contains 60 tablets and is for prescription use only. Storage instructions indicate to keep at 25°C with permitted excursions and to protect from light and moisture. The label also features manufacturer information and a barcode.*

* 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.