NDC 58657-504 – Guaifenesin and Dextromethorphan Hydrobromide
Dextromethorphan Hydrobromide 10 mg/5mL; Guaifenesin 100 mg/5mL · Syrup · Oral
Product NDC58657-504
Product details
- Brand name
- Guaifenesin and Dextromethorphan Hydrobromide
- Generic name
- Guaifenesin and Dextromethorphan Hydrobromide
- Labeler
- Method Pharmaceuticals
- Dosage form
- Syrup
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- April 1, 2024
- 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 Guaifenesin and Dextromethorphan Hydrobromide →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 58657-504-08 | 237 mL in 1 BOTTLE, PLASTIC (58657-504-08) | Apr 1, 2024 |
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- 51316-600 Guaifenesin 1200 mg/1; Dextromethorphan Hydrobromide 60 mg/1 · Tablet, Extended Release · CVS PHARMACY, INC
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