Active Ingredient (In Each Tablet/Caplet)
Naproxen sodium USP, 220 mg
(naproxen USP, 200 mg) (NSAID)
nonsteroidal anti-inflammatory drug
The following Structured Product Label (SPL) was submitted to the FDA by Dr.reddy's Laboratories Limited for the product Naproxen Sodium (NDC 55111-272). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet/caplet), purposes, uses, directions, other information, inactive ingredients, questions?, package label.principal display panel section, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Naproxen sodium USP, 220 mg
(naproxen USP, 200 mg) (NSAID)
nonsteroidal anti-inflammatory drug
Pain reliever/fever reducer
| Adults and children 12 years and older |
|
| Children under 12 years |
|
FD&C blue no. 2, hypromellose, magnesium stearate, microcrystalline cellulose, polyethylene glycol, polysorbate 80, povidone, talc, titanium dioxide
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