Drugplain

Mucus Relief Extended Release Maximum Strength 1200 mg/1

Guaifenesin · TABLET · CARDINAL HEALTH 110, LLC. DBA LEADER 70000

No Recall History
Plain English

Mucus Relief Extended Release Maximum Strength is a tablet containing guaifenesin at 1200 mg/1, taken oral. Manufactured by CARDINAL HEALTH 110, LLC. DBA LEADER 70000.

Key Facts

Brand Name
Mucus Relief Extended Release Maximum Strength
Generic Name
Guaifenesin
NDC Code (Product)
70000-0479
Manufacturer
CARDINAL HEALTH 110, LLC. DBA LEADER 70000
Strength
1200 mg/1
Dosage Form
TABLET
Route
ORAL
Marketing Status
Application #
ANDA207342
Drug Class
Expectorant [EPC]
Marketing Start
01/31/2019

Recall History

No Recall History

Side Effects Reported to FDA

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

dyspnoea549 reports
pneumonia517 reports
nausea469 reports
fatigue438 reports
pain420 reports
drug ineffective416 reports
diarrhoea391 reports
cough360 reports
off label use360 reports
headache357 reports

Frequently Asked Questions

What is Mucus Relief Extended Release Maximum Strength used for?

Mucus Relief Extended Release Maximum Strength contains Guaifenesin. It is a tablet taken oral. Consult your doctor for specific uses.

Is Mucus Relief Extended Release Maximum Strength a controlled substance?

Mucus Relief Extended Release Maximum Strength is not classified as a controlled substance by the DEA.

What is the generic name for Mucus Relief Extended Release Maximum Strength?

The generic name for Mucus Relief Extended Release Maximum Strength is Guaifenesin. There are 12 other brand versions of Guaifenesin.

What is the NDC code for Mucus Relief Extended Release Maximum Strength 1200 mg/1?

The NDC (National Drug Code) for Mucus Relief Extended Release Maximum Strength 1200 mg/1 is 70000-0479, listed by CARDINAL HEALTH 110, LLC. DBA LEADER 70000.