NDC 69729-812 – DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL · Syrup · Oral
Product NDC69729-812
Product details
- Brand name
- DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
- Generic name
- DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
- Labeler
- OPMX LLC
- Dosage form
- Syrup
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- October 15, 2025
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Dextromethorphan Hydrobromide 10 mg/5mL
- Guaifenesin 100 mg/5mL
Uses, dosage, side effects and warnings for DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 69729-812-04 | 118 mL in 1 BOTTLE (69729-812-04) | Oct 15, 2025 |
Other DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN products
- 85722-0001 Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL · Syrup · KJD Pharma Private Limited
- 85722-0002 Dextromethorphan Hydrobromide 20 mg/5mL; Guaifenesin 300 mg/5mL · Syrup · KJD Pharma Private Limited
- 69729-020 Dextromethorphan Hydrobromide 20 mg/5mL; Guaifenesin 300 mg/5mL · Syrup · OPMX LLC
- 69729-035 Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL · Syrup · OPMX LLC
- 69729-036 Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL · Syrup · OPMX LLC
- 69729-040 Dextromethorphan Hydrobromide 20 mg/5mL; Guaifenesin 300 mg/5mL · Syrup · OPMX LLC
- 69729-062 Dextromethorphan Hydrobromide 20 mg/5mL; Guaifenesin 300 mg/5mL · Syrup · OPMX LLC
- 69729-069 Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL · Syrup · OPMX LLC