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Brontuss
Brontuss - 49963-381-04 - (Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride)
Drug Information of Brontuss
| Product NDC: | 49963-381 |
| Proprietary Name: | Brontuss |
| Non Proprietary Name: | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Active Ingredient(s): | 15; 300; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Brontuss
| Product NDC: | 49963-381 |
| Labeler Name: | Portal Pharmaceutical |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20111222 |
Package Information of Brontuss
| Package NDC: | 49963-381-04 |
| Package Description: | 118 mL in 1 BOTTLE (49963-381-04) |
NDC Information of Brontuss
| NDC Code | 49963-381-04 |
| Proprietary Name | Brontuss |
| Package Description | 118 mL in 1 BOTTLE (49963-381-04) |
| Product NDC | 49963-381 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20111222 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Portal Pharmaceutical |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 15; 300; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
