Naproxen 500 MG Delayed Release Oral Tablet
INDICATIONS AND USAGE Carefully consider the potential benefits and risks of Naproxen delayed-release tablets and other treatment options before deciding to use naproxen delayed-release tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). Naproxen delayed-release tablets are indicated: For the relief of the signs and symptoms of rheumatoid arthritis For the relief of the signs and symptoms of osteoarthritis For the relief of the signs and symptoms of ankylosing spondylitis For the relief of the signs and symptoms of juvenile arthritis Naproxen delayed-release tablets are not recommended for initial treatment of acute pain because the absorption of naproxen is delayed compared to absorption from other naproxen-containing products (see CLINICAL PHARMACOLOGY and DOSAGE AND ADMINISTRATION ).
camber pharmaceuticals
OVAL WHITE I 11
I 11 OVAL WHITE
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HOW SUPPLIED Naproxen Delayed-release Tablets USP: 375 mg: white Enteric coated, capsule-shaped, biconvex tablets de-bossed with ‘I 1’ on one side, supplied in bottles of 100’s count (NDC 31722-338-01). Naproxen Delayed-release Tablets USP: 500 mg: white Enteric coated, capsule-shaped, biconvex tablets de-bossed with ‘I 11’ on one side, supplied in bottles of 100’s count (NDC 31722-339-01) and 500’s count (NDC 31722-339-05). Store at 20° to 25°C (68° to 77°F); [See USP Controlled Room Temperature]. Dispense in tight, lightÂresistant containers.
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