Drugplain

naproxen sodium 220 mg/1

Naproxen sodium · TABLET, FILM COATED · H E B

No Recall History
Plain English

naproxen sodium is a tablet, film coated containing naproxen sodium at 220 mg/1, taken oral. Manufactured by H E B.

Key Facts

Brand Name
naproxen sodium
Generic Name
Naproxen sodium
NDC Code (Product)
37808-631
Manufacturer
H E B
Strength
220 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA074661
Marketing Start
11/14/2017

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective2,884 reports
fatigue2,621 reports
off label use2,511 reports
pain2,461 reports
rash2,240 reports
arthralgia2,199 reports
diarrhoea2,199 reports
vomiting2,128 reports
condition aggravated2,101 reports
joint swelling2,057 reports

Frequently Asked Questions

What is naproxen sodium used for?

naproxen sodium contains Naproxen sodium. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is naproxen sodium a controlled substance?

naproxen sodium is not classified as a controlled substance by the DEA.

What is the generic name for naproxen sodium?

The generic name for naproxen sodium is Naproxen sodium. There are 11 other brand versions of Naproxen sodium.

What is the NDC code for naproxen sodium 220 mg/1?

The NDC (National Drug Code) for naproxen sodium 220 mg/1 is 37808-631, listed by H E B.