Source: FDA, National Drug Code (US) Revision Year: 2022
IBU tablets contain the active ingredient ibuprofen, which is (±)2(p-isobutylphenyl) propionic acid. Ibuprofen is a white powde rwith a melting point of 74-77°C and is very slightly soluble in water (<1 mg/mL) and readily soluble in organic solvents such as ethanol and acetone. The structural formula is represented below:
IBU, a nonsteroidal anti-inflammatory drug (NSAID), is available in 400 mg, 600 mg, and 800 mg tablets for oral administration. Inactive ingredients: carnauba wax, colloidal silicon dioxide, croscarmellose sodium, hypromellose, magnesium stearate, microcrystalline cellulose, polydextrose, polyethylene glycol, polysorbate, titanium dioxide.
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IBU tablets are available in the following strengths, colors and sizes: 600 mg (white, caplet, debossed 6I) Bottles of 100 NDC 66267-964-00 Manufactured by: Dr. Reddy’s Laboratories Louisiana, LLC, Shreveport, LA 71106 USA |
| Drug | Countries | |
|---|---|---|
| IBU | Turkey, United States |
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