Drugplain

Mucinex D 600 mg/1

Guaifenesin and Pseudoephedrine Hydrochloride · TABLET, EXTENDED RELEASE · Reckitt Benckiser LLC

No Recall History
Plain English

Mucinex D is a tablet, extended release containing guaifenesin and pseudoephedrine hydrochloride at 600 mg/1, taken oral. Manufactured by Reckitt Benckiser LLC.

Key Facts

Brand Name
Mucinex D
Generic Name
Guaifenesin and Pseudoephedrine Hydrochloride
NDC Code (Product)
63824-057
Manufacturer
Reckitt Benckiser LLC
Strength
600 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
NDA021585
Drug Class
Expectorant [EPC]
Marketing Start
06/26/2012

Recall History

No Recall History

Frequently Asked Questions

What is Mucinex D used for?

Mucinex D contains Guaifenesin and Pseudoephedrine Hydrochloride. It is a tablet, extended release taken oral. Consult your doctor for specific uses.

Is Mucinex D a controlled substance?

Mucinex D is not classified as a controlled substance by the DEA.

What is the generic name for Mucinex D?

The generic name for Mucinex D is Guaifenesin and Pseudoephedrine Hydrochloride. There are 11 other brand versions of Guaifenesin and Pseudoephedrine Hydrochloride.

What is the NDC code for Mucinex D 600 mg/1?

The NDC (National Drug Code) for Mucinex D 600 mg/1 is 63824-057, listed by Reckitt Benckiser LLC.