NDC 69367-184 – DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE
Dextromethorphan Hydrobromide 18 mg/15mL; Guaifenesin 200 mg/15mL; Phenylephrine Hydrochloride 10 mg/15mL · Liquid · Oral
Product NDC69367-184
Product details
- Brand name
- DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE
- Generic name
- DEXTROMETHORPHAN HYDROBROMIDE, Guaifenesin, and PHENYLEPHRINE HYDROCHLORIDE
- Labeler
- Westminster Pharmaceuticals, LLC
- Dosage form
- Liquid
- Route
- Oral
- Marketing category
- OTC MONOGRAPH DRUG · M012
- Marketed since
- March 15, 2018
- Listing expires
- December 31, 2026
- Pharmacologic class
- Expectorant; Sigma-1 Agonist; Uncompetitive N-methyl-D-aspartate Receptor Antagonist; alpha-1 Adrenergic Agonist
Active ingredients
- Dextromethorphan Hydrobromide 18 mg/15mL
- Guaifenesin 200 mg/15mL
- Phenylephrine Hydrochloride 10 mg/15mL
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 69367-184-08 | 240 mL in 1 BOTTLE (69367-184-08) | Mar 15, 2018 |