arthritis pain relief 650 mg/1

Acetaminophen · TABLET, FILM COATED, EXTENDED RELEASE · Publix Super Markets Inc

No Recall HistoryCurrently in Shortage

Plain English

arthritis pain relief is a tablet, film coated, extended release containing acetaminophen at 650 mg/1, taken oral. Manufactured by Publix Super Markets Inc.

Key Facts

Brand Name: arthritis pain relief
Generic Name: Acetaminophen
NDC Code (Product): 56062-544
Manufacturer: Publix Super Markets Inc
Strength: 650 mg/1
Dosage Form: TABLET, FILM COATED, EXTENDED RELEASE
Route: ORAL
Marketing Status
Application #: ANDA075077
Marketing Start: 11/26/2007

Recall History

No Recall History

Side Effects Reported to FDA

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

off label use24,964 reports

fatigue23,927 reports

drug ineffective22,772 reports

pain22,029 reports

nausea19,420 reports

headache18,455 reports

arthralgia16,263 reports

dyspnoea15,879 reports

toxicity to various agents15,654 reports

vomiting15,558 reports

Frequently Asked Questions

What is arthritis pain relief used for?

arthritis pain relief contains Acetaminophen. It is a tablet, film coated, extended release taken oral. Consult your doctor for specific uses.

Is arthritis pain relief a controlled substance?

arthritis pain relief is not classified as a controlled substance by the DEA.

What is the generic name for arthritis pain relief?

The generic name for arthritis pain relief is Acetaminophen. There are 12 other brand versions of Acetaminophen.

What is the NDC code for arthritis pain relief 650 mg/1?

The NDC (National Drug Code) for arthritis pain relief 650 mg/1 is 56062-544, listed by Publix Super Markets Inc.

Product NDC

56062-544

Package NDC

56062-544-62

Other Acetaminophen Brands

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Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)