Probenecid 500 mg/1
Probenecid · TABLET, FILM COATED · Actavis Pharma, Inc.
No Recall History
Plain English
Probenecid is a tablet, film coated containing probenecid at 500 mg/1, taken oral. Manufactured by Actavis Pharma, Inc..
Key Facts
- Brand Name
- Probenecid
- Generic Name
- Probenecid
- NDC Code (Product)
0591-5347- Manufacturer
- Actavis Pharma, Inc.
- Strength
- 500 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- ANDA084442
- Marketing Start
- 07/01/1983
Recall History
No Recall HistorySide Effects Reported to FDA
FDA FAERS database · These are reported events, not confirmed side effects
diarrhoea105 reports
drug ineffective66 reports
off label use59 reports
dyspnoea53 reports
nausea50 reports
vomiting49 reports
asthenia48 reports
adenovirus infection47 reports
fatigue47 reports
acute kidney injury45 reports
Frequently Asked Questions
What is Probenecid used for?
Probenecid contains Probenecid. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is Probenecid a controlled substance?
Probenecid is not classified as a controlled substance by the DEA.
What is the generic name for Probenecid?
The generic name for Probenecid is Probenecid. There are 4 other brand versions of Probenecid.
What is the NDC code for Probenecid 500 mg/1?
The NDC (National Drug Code) for Probenecid 500 mg/1 is 0591-5347, listed by Actavis Pharma, Inc..