Ibuprofen Tablet, Film Coated
Product Images NDC 49483-604

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 49483-604). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Time Cap Laboratories, 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

602r Ibuprofen 400 mg 100 Count Ng 15 301

602r Ibuprofen 400 mg 100 Count   Ng 15 301
Label for Ibuprofen Tablets, USP 400 mg oral tablets from Time-Cap Labs, Inc. The label indicates a package size of 100 tablets and includes storage instructions to keep at controlled room temperature. It mentions the product is manufactured by Marksans Pharma Ltd in India and has the NDC 49483-602-01. The label is primarily white with pink and purple accents and features a barcode.*
FDA Label Image

602r Ibuprofen 400 mg 500 Count Ng 15 302

602r Ibuprofen 400 mg 500 Count   Ng 15 302
Label for Ibuprofen tablets USP 400 mg by Time-Cap Labs, Inc., containing 500 film-coated oral tablets. The label includes dosage and use instructions, storage temperature (20° to 25°C), barcode, and manufacturer information (Marksans Pharma Ltd., Goa, India). The label also notes dispensing guidance for pharmacists.*
FDA Label Image

603r Ibuprofen 600 mg 100 Count Ng 15 305

603r Ibuprofen 600 mg 100 Count   Ng 15 305
Label for Ibuprofen Tablets USP 600 mg film-coated tablets by Time-Cap Labs, Inc. The label includes the quantity of 100 tablets, marked Rx only, with storage instructions and manufacturer information. The label is predominantly white with orange and green accents and includes a barcode.*
FDA Label Image

603r Ibuprofen 600 mg 500 Count Ng 15 306

603r Ibuprofen 600 mg 500 Count   Ng 15 306
Label for Ibuprofen Tablets, USP 600 mg from Time-Cap Labs, Inc. The label states the product is film-coated tablets, Rx only, and contains 500 capsule-shaped tablets. It includes storage instructions and manufacturer details for Marksans Pharma Ltd., India. The label bears the NDC number 49483-603-50.*
FDA Label Image

604r Ibuprofen 800 mg 100 Count Ng 15 309

604r Ibuprofen 800 mg 100 Count   Ng 15 309
Label for Ibuprofen Tablets, USP, 800 mg, film-coated tablets, manufactured by Marksans Pharma Ltd and labeled by Time-Cap Labs, Inc. The package contains 100 capsule-shaped tablets. Storage instructions and dispensing information are included, along with a barcode and manufacturer addresses in the USA and India.*
FDA Label Image

604r Ibuprofen 800 mg 500 Count Ng 15 310

604r Ibuprofen 800 mg 500 Count   Ng 15 310
Label for Ibuprofen Tablets, USP 800 mg by Time Cap Labs, Inc. The label shows a pack size of 500 capsule-shaped tablets with NDC 49483-604-50. It includes storage instructions and manufacturer details, indicating manufacturing by Marksans Pharma Ltd., India. The label emphasizes dispensing with a medication guide and storing at controlled room temperature.*
FDA Label Image

Medication Guide For Nonsteroidal Anti Inflammatory Drugs

Medication Guide For Nonsteroidal Anti Inflammatory Drugs
This image shows a Medication Guide text for Nonsteroidal Anti-Inflammatory Drugs (NSAIDs), describing important safety information, possible side effects, usage warnings, and precautions for NSAIDs, including Ibuprofen. It includes detailed guidance on who should or should not take NSAIDs, symptoms requiring emergency attention, and contact information for reporting side effects. Manufacturer details for Time-Cap Labs, Inc. and Marksans Pharma Ltd. are included at the bottom.*

* 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.