Drugplain

MUCINEX D 600 mg/1

Guaifenesin and Pseudoephedrine Hydrochloride · TABLET, EXTENDED RELEASE · A-S Medication Solutions

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 A-S Medication Solutions.

Key Facts

Brand Name
MUCINEX D
Generic Name
Guaifenesin and Pseudoephedrine Hydrochloride
NDC Code (Product)
50090-1076
Manufacturer
A-S Medication Solutions
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

Side Effects Reported to FDA

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

drug ineffective147 reports
insomnia147 reports
dizziness129 reports
headache113 reports
nausea107 reports
fatigue102 reports
dyspnoea86 reports
accidental overdose76 reports
cough73 reports
sinusitis71 reports

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 50090-1076, listed by A-S Medication Solutions.