NDC 85722-0002 – DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
Dextromethorphan Hydrobromide 20 mg/5mL; Guaifenesin 300 mg/5mL · Syrup · Oral
Product NDC85722-0002
Product details
- Brand name
- DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
- Generic name
- DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
- Labeler
- KJD Pharma Private Limited
- Dosage form
- Syrup
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- February 1, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist
Active ingredients
- Dextromethorphan Hydrobromide 20 mg/5mL
- Guaifenesin 300 mg/5mL
Uses, dosage, side effects and warnings for DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 85722-0002-4 | 118 mL in 1 BOTTLE (85722-0002-4) | Feb 1, 2021 |
| 85722-0002-6 | 473 mL in 1 BOTTLE (85722-0002-6) | Feb 1, 2021 |
| 85722-0002-8 | 236 mL in 1 BOTTLE (85722-0002-8) | Feb 1, 2021 |
Other DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN products
- 85722-0001 Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 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
- 69729-812 Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL · Syrup · OPMX LLC