Ibuprofen Capsule, Liquid Filled
Product Images NDC 59556-895

2 FDA label images from Strides Pharma Inc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 59556-895). 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.

Product Images & Figures Index

FDA Label Image

Ibuprofen Container Label (5f77c518 6b51 4074 Bce0 Bcefa3129ad6 01)

Ibuprofen Container Label (5f77c518 6b51 4074 Bce0 Bcefa3129ad6 01)
Ibuprofen Capsules 200 mg liquid-filled capsules label by Strides Pharma Inc. The label shows the active ingredient as solubilized ibuprofen, each capsule containing 200 mg as NSAID. The product is intended as a pain reliever and fever reducer, with 80 liquid-filled capsules per package. Packaging includes usage warnings and manufacturer details from Strides Shasun Limited, India, with distribution in East Brunswick, NJ.*
FDA Label Image

Ibuprofen Carton Label (5f77c518 6b51 4074 Bce0 Bcefa3129ad6 02)

Ibuprofen Carton Label (5f77c518 6b51 4074 Bce0 Bcefa3129ad6 02)
Packaging label for Ibuprofen Liquid Gels 200 mg by Strides Pharma Inc. The label identifies the product as solubilized ibuprofen capsules, liquid filled, containing 200 mg of the active ingredient per capsule. The package contains 80 liquid-filled capsules. It is labeled as a pain reliever and fever reducer (NSAID). The label includes drug facts, warnings, directions, inactive ingredients, barcodes, and contact information for questions or comments.*

* 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.