Over-the-counter drug · ANDA
Mucus Relief - DM Maximum Strength (Guaifenesin, dextromethorphan hbr) NDC 73581-405
Dextromethorphan hydrobromide 60 mg/1; Guaifenesin 1200 mg/1 · Tablet, Extended release · Oral · YYBA CORP
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 73581-405-98 | 7358104059873581040598 | 98 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (73581-405-98)Marketed from Apr 1, 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 - DM Maximum StrengthSuffix: MAXIMUM STRENGTH
- Generic name (nonproprietary)
- guaifenesin, dextromethorphan hbr
- Active ingredients
- Dextromethorphan hydrobromide — 60 mg/1Guaifenesin — 1200 mg/1
- Dosage form
- Tablet, Extended release
- Route
- Oral
- Labeler
- YYBA CORPNDC labeler code 73581
- Product type
- Over-the-counter drug
- Marketing category
- ANDA — Abbreviated New Drug Application (generic)Application ANDA 214781
- 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 73581-405_3ce33efd-e300-a7e2-e063-6394a90ad2c1SPL ID 3ce33efd-e300-a7e2-e063-6394a90ad2c1SPL set ID 325b5e55-ba58-312c-e063-6394a90aee55RxCUI 1099074UNII 9D2RTI9KYH, 495W7451VQUPC 0373581000715
- 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
N473581040598followed by a unit qualifier and the quantityPackage 73581-0405-98. 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 73581-405
- What is NDC 73581-405?
- 73581-405 is the product NDC for Mucus Relief - DM Maximum Strength, Dextromethorphan hydrobromide 60 mg/1; Guaifenesin 1200 mg/1 tablet, extended release, listed with the FDA by YYBA CORP. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Mucus Relief - DM Maximum Strength (Guaifenesin, Dextromethorphan HBr).
- What is the active ingredient?
- Dextromethorphan hydrobromide, Guaifenesin.
- Who is the labeler?
- YYBA CORP, NDC labeler code 73581. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Mucus Relief - DM Maximum Strength?
- 8 other product NDCs are listed under this name. See all Mucus Relief - DM Maximum Strength NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Mucus Relief - DM Maximum Strength products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Mucus Relief - DM Maximum Strengthguaifenesin, dextromethorphan hbr | Dextromethorphan hydrobromide 60 mg/1; Guaifenesin 1200 mg/1 | TabletOral | YYBA CORP | 73581-406 | 73581-0406-0173581-0406-05 |
| Mucus Relief DM Maximum Strengthdextromethorphan hydrobromide guaifenesin | Dextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 400 mg/20mL | LiquidOral | CVS Pharmacy | 69842-904 | 69842-0904-06 |
| Mucus Relief DM Maximum Strengthdextromethorphan hbr and guaifenesin | Dextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 400 mg/20mL | SolutionOral | WALGREENS CO | 0363-7390 | 00363-7390-06 |
| Mucus Relief DM Maximum Strengthguaifenesin, dextromethorphan hbr | Dextromethorphan hydrobromide 60 mg/1; Guaifenesin 1200 mg/1 | TabletOral | Chain Drug Consortium, LLC | 68016-674 | 68016-0674-1468016-0674-28 |
| Mucus Relief DM Maximum Strengthdextromethorphan hbr and guaifenesin | Dextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 400 mg/20mL | SolutionOral | WINCO FOODS, LLC | 67091-342 | 67091-0342-06 |
| Mucus Relief DM Maximum Strengthguaifenesin, dextromethorphan hbr | Dextromethorphan hydrobromide 60 mg/1; Guaifenesin 1200 mg/1 | TabletOral | Rite Aid Corporation | 11822-7340 | 11822-7340-04 |
| Mucus Relief DM MAXIMUM STRENGTHguaifenesin and dextromethorphan hbr | Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1 | Tablet, Extended releaseOral | Better Living Brands LLC | 21130-989 | 21130-0989-0321130-0989-65 |
| Mucus Relief DM Maximum Strengthdextromethorphan hbr, guaifenesin | Dextromethorphan hydrobromide 20 mg/20mL; Guaifenesin 400 mg/20mL | LiquidOral | Dolgencorp, Inc. (DOLLAR GENERAL & REXALL) | 55910-505 | 55910-0505-08 |
Other NDCs under ANDA 214781
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 |
|---|---|---|---|---|
| Guaifenesin And Dextromethorphan HBr | Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1 | Tablet, Extended releaseOral | Kroger Company | 30142-948 |
| Guaifenesin And Dextromethorphan HBr | Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1 | Tablet, Extended releaseOral | Kroger Company | 30142-963 |
| Guaifenesin and Dextromethorphan HBr | Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1 | Tablet, Extended releaseOral | OHM LABORATORIES INC | 51660-110 |
| Guaifenesin and Dextromethorphan HBr | Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1 | Tablet, Extended releaseOral | OHM LABORATORIES INC | 51660-301 |
| Guaifenesin and Dextromethorphan HBr | Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1 | Tablet, Extended releaseOral | SUN PHARMACEUTICAL INDUSTRIES, INC. | 63304-106 |
| Guaifenesin and Dextromethorphan HBr | Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1 | Tablet, Extended releaseOral | SUN PHARMACEUTICAL INDUSTRIES, INC. | 63304-110 |
| Guaifenesin and Dextromethorphan Hydrobromide HBRguaifenesin and dextromethorphan hydrobromide | Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1 | Tablet, Extended releaseOral | RITE-AID | 11822-9996 |
| Guaifenesin and Dextromethorphan HBr | Guaifenesin 600 mg/1; Dextromethorphan hydrobromide 30 mg/1 | Tablet, Extended releaseOral | PUBLIX SUPER MARKETS, INC | 41415-998 |
| Guaifenesin and Dextromethorphan HBr | Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1 | Tablet, Extended releaseOral | PUBLIX SUPER MARKETS, INC | 41415-999 |
| Guaifenesin and Dextromethorphan Hydrobromide | Guaifenesin 1200 mg/1; Dextromethorphan hydrobromide 60 mg/1 | Tablet, Extended releaseOral | CVS PHARMACY, INC | 51316-600 |