NDC codes

FDA NDC Directory
Product NDC (as listed)68391-724Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68391-0724Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
68391-724-95683910724951 BOTTLE in 1 CARTON (68391-724-95) / 84 TABLET, EXTENDED RELEASE in 1 BOTTLEMarketed from Aug 20, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Mucus Relief
Generic name (nonproprietary)
guaifenesin
Active ingredients
Guaifenesin — 1200 mg/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Over-the-counter drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217780
Marketing start
Listing expires
Other FDA classes
Decreased Respiratory Secretion Viscosity (Physiologic effect)Increased Respiratory Secretions (Physiologic effect)
Identifiers
Product ID 68391-724_3c120ab9-89a6-a9be-e063-6294a90a2b7cSPL ID 3c120ab9-89a6-a9be-e063-6294a90a2b7cSPL set ID 2f32e8f9-260c-fa36-e063-6294a90a953dRxCUI 310621UNII 495W7451VQUPC 0888670204030
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

N468391072495 followed by a unit qualifier and the quantity

Package 68391-0724-95. 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

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Uses helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 217780

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

FDA NDC Directory listings under ANDA 217780
ProductStrengthForm · routeLabelerProduct NDC
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralCVS Pharmacy51316-724
Guaifenesin Extended Release 600 mgguaifenesinGuaifenesin 600 mg/1TabletOralTIME CAP LABORATORIES, INC.49483-723
Guaifenesin Extended Release 1200 mgguaifenesinGuaifenesin 1200 mg/1TabletOralTIME CAP LABORATORIES, INC.49483-724
Mucus Relief ERguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralRugby Laboratories0536-1249
Guaifenesin 600 mgGuaifenesin 600 mg/1TabletOralMARKSANS PHARMA LIMITED25000-042
Guaifenesin 1200 mgGuaifenesin 1200 mg/1TabletOralMARKSANS PHARMA LIMITED25000-041
Maximum Strength Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralSAM'S WEST INC68196-033
Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralLEADER/ Cardinal Health 110, Inc.70000-0730
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralGrocery Outlet, Inc.85828-723
Mucus ReliefguaifenesinGuaifenesin 600 mg/1Tablet, Extended releaseOralKROGER COMPANY41226-723
Maximum Strength Mucus ReliefguaifenesinGuaifenesin 1200 mg/1Tablet, Extended releaseOralKROGER COMPANY41226-724

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