Mucinex DM Maximum Strength NDC 63824-072

Product information

Brand name (proprietary)

Mucinex DM Maximum StrengthSuffix: Maximum Strength

Generic name (nonproprietary)

guaifenesin and dextromethorphan hydrobromide

Active ingredients

Guaifenesin — 1200 mg/1Dextromethorphan hydrobromide — 60 mg/1

Dosage form

Tablet, Extended release

Route

Oral

Labeler

Reckitt Benckiser LLC

Product type

Over-the-counter drug

Marketing category

NDA — New Drug ApplicationApplication NDA 021620

Marketing start

Jun 26, 2012

Listing expires

Dec 31, 2027

Other FDA classes

Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)Sigma-1 Receptor Agonists (Mechanism)Uncompetitive NMDA Receptor Antagonists (Mechanism)

Identifiers

Product ID 63824-072_52d14310-1cbd-5cbb-e063-6294a90ade4aSPL ID 52d14310-1cbd-5cbb-e063-6294a90ade4aSPL set ID 588eddc1-fa30-41cc-8ed9-c01319ea21c6RxCUI 1099074UNII 495W7451VQ, 9D2RTI9KYHUPC 0363824072142

Pharmacologic class

Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N463824007202 followed by a unit qualifier and the quantity Copy

Package 63824-0072-02. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under NDA 021620

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.