Ibuprofen Tablet, Film Coated
Product Images NDC 68071-5135

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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Ibuprofen (NDC 68071-5135). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare 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

Pdp (68071 5135 0)

Pdp (68071 5135 0)
This is a medication bottle of Ibuprofen 800mg containing 100 tablets from NuCare Pharmaceuticals, Inc. The National Drug Code is 68071-5135-0, and the product's identification number is R0285100. The lot number is 000000, and the manufacturer's NDC is 49483-604-01 with an expiration date of 00-00. The bottle warns to keep out of reach from children and advises consumers to seek medical advice for any possible side effects. The recommended storage conditions of the medication at 68-77°F.*
FDA Label Image

Medguide Ibuprofen Tablets (Medication Guide For Nonsteroidal Anti Inflammatory Drugs)

Medguide Ibuprofen Tablets (Medication Guide For Nonsteroidal Anti Inflammatory Drugs)
This is a medication guide for Nonsteroidal Anti-Inflammatory Drugs (NSAIDs) that are used to treat pain, inflammation and redness from conditions such as different types of arthritis and menstrual cramps. NSAIDs can cause serious side effects such as increased risk of a heart attack, stroke, bleeding, ulcers and tears of the esophagus, stomach and intestines that can cause death. Patients should take NSAIDs exactly as prescribed, at the lowest dose possible for their treatment, and for the shortest time needed. Before taking NSAIDs, patients should inform their healthcare provider about their medical conditions and all of the medicines they take, including prescription, over-the-counter and herbal supplements, to avoid serious side effects. Patients should not use NSAIDs for more than 10 days without consulting their healthcare provider. The medication guide was approved by the U.S. Food and Drug Administration and manufactured by Time-Cap Labs, Inc. and Marksans Pharma Ltd.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.