Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride 69367-0184
Product NDC
69367-0184- Manufacturer
- Westminster Pharmaceuticals, Llc
- Dosage Form
- Liquid
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- March 15, 2018
- Listing Expires
- December 31, 2026
- Application
- M012
Active Ingredients
| Ingredient | Strength |
|---|---|
| Dextromethorphan Hydrobromide | 18 mg/15mL |
| Guaifenesin | 200 mg/15mL |
| Phenylephrine Hydrochloride | 10 mg/15mL |
Drug Class
Expectorant [EPC]Adrenergic alpha1-Agonists [MoA]Decreased Respiratory Secretion Viscosity [PE]
Packaging Options(1)
240 mL in 1 BOTTLE (69367-184-08)
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All Dextromethorphan Hydrobromide, Guaifenesin, And Phenylephrine Hydrochloride NDC codes →External Resources