Mucinex Maximum Strength (guaifenesin) NDC 50090-2301

Product information

Brand name (proprietary)

Mucinex Maximum StrengthSuffix: Maximum Strength

Generic name (nonproprietary)

guaifenesin

Active ingredients

Guaifenesin — 1200 mg/1

Dosage form

Tablet, Extended release

Route

Oral

Labeler

A-S Medication Solutions

Product type

Over-the-counter drug

Marketing category

NDA — New Drug ApplicationApplication NDA 021282

Marketing start

Jun 26, 2012

Listing expires

Dec 31, 2026

Other FDA classes

Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)

Identifiers

Product ID 50090-2301_30356fcf-98ca-4679-9c38-90864862a276SPL ID 30356fcf-98ca-4679-9c38-90864862a276SPL set ID 7e09314c-3421-4053-a2ac-b67bf5610f83RxCUI 310621, 891297UNII 495W7451VQ

Pharmacologic class

Expectorant

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

N450090230101 followed by a unit qualifier and the quantity Copy

Package 50090-2301-01. 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

Other NDCs under NDA 021282

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