Ibuprofen Tablet
Product Images NDC 62207-321

6 FDA label images from Granules India Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 62207-321). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Granules India Limited, 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

62207 320 46 250s Bottle Label Round

62207 320 46 250s Bottle Label Round
Drug Facts label for Ibuprofen Tablets USP 200 mg oral tablets by Granules India Limited. The label details active ingredient, NSAID uses for pain relief and fever reduction, allergy alerts, stomach bleeding warnings, directions, and storage information. The label includes the manufacturer and distributor information and a barcode.*
FDA Label Image

62207 320 46 250s Carton Round

62207 320 46 250s Carton Round
IBUPROFEN 200 mg coated tablets packaging label from Granules India Limited. The label includes drug facts, warnings, directions, and ingredient information. It states that each tablet contains 200 mg of ibuprofen, a nonsteroidal anti-inflammatory drug (NSAID). The packaging design is mostly white with teal and black text, including sections with warnings, uses, and directions for safe medication use.*
FDA Label Image

62207-320-91-bulk-label-jpg (62207 320 91 Bulk Label Jpg)

62207-320-91-bulk-label-jpg (62207 320 91 Bulk Label Jpg)
This image shows a product information label for Ibuprofen Tablets USP 200 mg. It lists the active ingredient ibuprofen 200 mg per tablet, batch number, manufacturing and expiration dates (placeholders), NDC number 62207-320-91, manufacturer Granules India Limited along with its address in Telangana, India. The label includes storage instructions and cautions, and displays barcodes and packaging details such as number of units (160,000).*
FDA Label Image

62207-321-46-250s-bottle-label.jpg (62207 321 46 250s Bottle Label)

62207-321-46-250s-bottle-label.jpg (62207 321 46 250s Bottle Label)
Drug Facts label for Ibuprofen Tablets, USP 200 mg oral tablets by Granules India Limited. The label includes active ingredient and purpose, uses, warnings including allergy alert and stomach bleeding warning, directions for use, and additional safety information. The label also states product contains no gluten ingredients and provides manufacturer and distributor details. The design features text blocks, a barcode, and instructions to read product information before use.*
FDA Label Image

62207-321-46-250s-carton.jpg (62207 321 46 250s Carton)

62207-321-46-250s-carton.jpg (62207 321 46 250s Carton)
Box packaging label for IBUPROFEN 200 mg tablets USP by Granules India Limited. The label shows 250 coated caplets in a capsule-shaped tablet form. It includes Drug Facts such as active ingredient, uses, warnings, directions, inactive ingredients, and storage information. The product is identified as an oral pain reliever and fever reducer (NSAID), distributed by Granules USA, Inc.*
FDA Label Image

62207-321-91-bulk-label-jpg (62207 321 91 Bulk Label Jpg)

62207-321-91-bulk-label-jpg (62207 321 91 Bulk Label Jpg)
Label for Ibuprofen Tablets USP 200 mg (Caplet) showing that each film-coated tablet contains 200 mg of ibuprofen. The label includes batch number, manufacturing date, expiry date, NDC number 62207-321-91, manufacturing license number, and storage instructions to keep between 20-25°C (68-77°F). It notes the product is for repacking only, and is manufactured by Granules India Limited, Telangana, India, with address and barcodes present.*

* 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.