Over-the-counter drug · NDA
Mucinex DM NDC 85766-176
guaifenesin and dextromethorphan hydrobromide · Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1 · Tablet, Extended release · Oral · Sportpharm LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 85766-176-20 | 8576601762085766017620 | 1 BLISTER PACK in 1 CARTON (85766-176-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Feb 27, 2026 | |
| 85766-176-40 | 8576601764085766017640 | 2 BLISTER PACK in 1 CARTON (85766-176-40) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Feb 27, 2026 | |
| 85766-176-60 | 8576601766085766017660 | 3 BLISTER PACK in 1 CARTON (85766-176-60) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMarketed from Feb 27, 2026 |
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)
- guaifenesin and dextromethorphan hydrobromide
- Active ingredients
- Guaifenesin — 600 mg/1Dextromethorphan hydrobromide — 30 mg/1
- Dosage form
- Tablet, Extended release
- Route
- Oral
- Labeler
- Sportpharm LLCNDC labeler code 85766
- Product type
- Over-the-counter drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 021620
- Marketing start
- Listing expires
- 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 85766-176_4bc7e1b5-c896-c837-e063-6294a90a475aSPL ID 4bc7e1b5-c896-c837-e063-6294a90a475aSPL set ID 8f4af6dd-6df4-49a7-98cf-655136923734RxCUI 1298324UNII 495W7451VQ, 9D2RTI9KYH
- 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
N485766017620followed by a unit qualifier and the quantityPackage 85766-0176-20. 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 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.
About NDC 85766-176
- What is NDC 85766-176?
- 85766-176 is the product NDC for Mucinex DM, Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1 tablet, extended release, listed with the FDA by Sportpharm LLC. It has 3 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Mucinex DM (Guaifenesin and Dextromethorphan Hydrobromide).
- What is the active ingredient?
- Guaifenesin, Dextromethorphan hydrobromide.
- Who is the labeler?
- Sportpharm LLC, NDC labeler code 85766. 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.
Related NDCs: other Mucinex DM products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Mucinex DMdextromethorphan hydrobromide, guaifenesin | Dextromethorphan hydrobromide 30 mg/1; Guaifenesin 600 mg/1 | Tablet, Extended releaseOral | Navajo Manufacturing Company Inc. | 67751-171 | 67751-0171-01 |
| 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 | 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.
| 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 DMdextromethorphan hydrobromide, guaifenesin | Dextromethorphan hydrobromide 30 mg/1; Guaifenesin 600 mg/1 | Tablet, Extended releaseOral | Navajo Manufacturing Company Inc. | 67751-171 |
| Mucinex DMguaifenesin and dextromethorphan hydrobromide | Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1 | Tablet, Extended releaseOral | Select Consumer Group | 85237-1650 |
| 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 |