What is NDC 67751-171?

67751-171 is the product NDC for Mucinex DM, Dextromethorphan hydrobromide 30 mg/1; Guaifenesin 600 mg/1 tablet, extended release, listed with the FDA by Navajo Manufacturing Company Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Mucinex DM (Dextromethorphan hydrobromide, Guaifenesin).

What is the active ingredient?

Dextromethorphan hydrobromide, Guaifenesin.

Navajo Manufacturing Company Inc., NDC labeler code 67751. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Mucinex DM?

6 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Mucinex DM NDC 67751-171 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)67751-171Labeler and product segments. Claims need a package NDC.

Product NDC at billing width67751-0171Add 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 NDC	11-digit (billing)	Package	Copy
67751-171-01	6775101710167751017101	1 POUCH in 1 CARTON (67751-171-01) / 2 TABLET, EXTENDED RELEASE in 1 POUCHMarketed from Sep 23, 2016

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): Mucinex DM
Generic name (nonproprietary): dextromethorphan hydrobromide, guaifenesin
Active ingredients: Dextromethorphan hydrobromide — 30 mg/1Guaifenesin — 600 mg/1
Dosage form: Tablet, Extended release
Route: Oral
Labeler: Navajo Manufacturing Company Inc.NDC labeler code 67751
Product type: Over-the-counter drug
Marketing category: NDA — New Drug ApplicationApplication NDA 021620
Marketing start: Sep 23, 2016
Listing expires: Dec 31, 2026
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 67751-171_f70e0eb0-95aa-645c-e053-6394a90aae83SPL ID f70e0eb0-95aa-645c-e053-6394a90aae83SPL set ID 4226f394-f85e-45b1-8d5f-7cffb7dd492fRxCUI 1298324UNII 9D2RTI9KYH, 495W7451VQ
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

N467751017101 followed by a unit qualifier and the quantity

Package 67751-0171-01. 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

Current FDA label (SPL), effective Mar 16, 2023.

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 temporarily relieves: cough due to minor throat and bronchial irritation as may occur with the common cold or inhaled irritants the intensity of coughing the impulse to cough to help you get to sleep

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67751-171

What is NDC 67751-171?: 67751-171 is the product NDC for Mucinex DM, Dextromethorphan hydrobromide 30 mg/1; Guaifenesin 600 mg/1 tablet, extended release, listed with the FDA by Navajo Manufacturing Company Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Mucinex DM (Dextromethorphan hydrobromide, Guaifenesin).
What is the active ingredient?: Dextromethorphan hydrobromide, Guaifenesin.
Who is the labeler?: Navajo Manufacturing Company Inc., NDC labeler code 67751. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Mucinex DM?: 6 other product NDCs are listed under this name. See all Mucinex DM NDCs.
Is there a related HCPCS / J-code?: Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Mucinex DM NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-1077	50090-1077-00
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-1078	50090-1078-00
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Reckitt Benckiser LLC	63824-056	63824-0056-3263824-0056-3463824-0056-36+4 more
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Select Consumer Group	85237-1650	85237-1650-0185237-1650-03
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Sportpharm LLC	85766-176	85766-0176-2085766-0176-4085766-0176-60
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Lil' Drug Store Products, Inc.	66715-9724	66715-9724-01

Other NDCs under NDA 021620

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

FDA NDC Directory listings under NDA 021620
Product	Strength	Form · route	Labeler	Product NDC
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-1077
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-1078
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Reckitt Benckiser LLC	63824-056
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Lil' Drug Store Products, Inc.	66715-9724
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Select Consumer Group	85237-1650
Mucinex DMguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Sportpharm LLC	85766-176
Mucinex DM Maximum Strengthguaifenesin and dextromethorphan hydrobromide	Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1	Tablet, Extended releaseOral	A-S Medication Solutions	50090-6549
Mucinex DM Maximum Strengthguaifenesin and dextromethorphan hydrobromide	Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1	Tablet, Extended releaseOral	Reckitt Benckiser LLC	63824-072
Mucinex DM, CVP HEALTHguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Lil' Drug Store Products, Inc.	66715-6524
Mucinex DM, TRAVEL BASIXguaifenesin and dextromethorphan hydrobromide	Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1	Tablet, Extended releaseOral	Lil' Drug Store Products, Inc.	66715-6424