Ibuprofen
Product Images NDC 42543-966

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 42543-966). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma 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

Chem Structure (C3f2b181 D310 4a4b Bb46 172c49d4b7e3 01)

Chemical structure of Ibuprofen showing its molecular arrangement with specific atoms and bonds including a benzene ring and carboxyl group.*

FDA Label Image

400 mg Label (C3f2b181 D310 4a4b Bb46 172c49d4b7e3 02)

The label for Ibuprofen Tablets, USP 400 mg film-coated tablets by Strides Pharma Inc. It indicates the product contains 500 tablets, is for prescription use only, and provides storage instructions. The label also includes manufacturer and distributor information, batch details space, and emphasizes keeping the medication out of children's reach.*

FDA Label Image

600 mg Label (C3f2b181 D310 4a4b Bb46 172c49d4b7e3 03)

Label for Ibuprofen Tablets, USP 600 mg by Strides Pharma Inc. The label indicates 500 tablets in the package with storage instructions and warnings. Manufacturer is Strides Pharma Global Pte. Ltd., Singapore, and the distributor is Strides Pharma Inc., East Brunswick, NJ. The label includes an NDC code 42543-965-07 and barcode.*

FDA Label Image

800 mg Label (C3f2b181 D310 4a4b Bb46 172c49d4b7e3 04)

Label for Ibuprofen Tablets, USP 800 mg, film-coated, supplied by Strides Pharma Inc. The label indicates a package size of 500 tablets, with storage instructions between 20°C to 25°C. It is marked Rx only and includes manufacturer details as Strides Pharma Global Pte. Ltd., Singapore.*

* 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.