Drugplain

PANADOL Extra 500 mg/1

acetaminophen and caffeine · TABLET, FILM COATED · Haleon US Holdings LLC

No Recall HistoryCurrently in Shortage
Plain English

PANADOL Extra is a tablet, film coated containing acetaminophen and caffeine at 500 mg/1, taken oral. Manufactured by Haleon US Holdings LLC.

Key Facts

Brand Name
PANADOL Extra
Generic Name
acetaminophen and caffeine
NDC Code (Product)
0135-0620
Manufacturer
Haleon US Holdings LLC
Strength
500 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
M013
Drug Class
Central Nervous System Stimulant [EPC]; Methylxanthine [EPC]
Marketing Start
03/01/2017

Recall History

No Recall History

Frequently Asked Questions

What is PANADOL Extra used for?

PANADOL Extra contains acetaminophen and caffeine. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is PANADOL Extra a controlled substance?

PANADOL Extra is not classified as a controlled substance by the DEA.

What is the generic name for PANADOL Extra?

The generic name for PANADOL Extra is acetaminophen and caffeine. There are 1 other brand versions of acetaminophen and caffeine.

What is the NDC code for PANADOL Extra 500 mg/1?

The NDC (National Drug Code) for PANADOL Extra 500 mg/1 is 0135-0620, listed by Haleon US Holdings LLC.

Product NDC

0135-0620

Package NDC

0135-0620-01

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

Data from openFDA · Public domain (CC0 1.0)