Glentuss is a Oral Syrup in the Human Otc Drug category. It is labeled and distributed by Glendale Inc. The primary component is Dextromethorphan Hydrobromide; Pseudoephedrine Hydrochloride; Doxylamine Succinate.
| Product ID | 70147-233_f23182eb-a618-4556-a265-3de318cc7ae5 |
| NDC | 70147-233 |
| Product Type | Human Otc Drug |
| Proprietary Name | Glentuss |
| Generic Name | Dextromethorphan Hydrobromide, Pseudoephedrine Hydrochloride, And Doxylamine Succinate |
| Dosage Form | Syrup |
| Route of Administration | ORAL |
| Marketing Start Date | 2015-12-05 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Glendale Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; PSEUDOEPHEDRINE HYDROCHLORIDE; DOXYLAMINE SUCCINATE |
| Active Ingredient Strength | 15 mg/5mL; mg/5mL; mg/5mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2015-12-05 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2015-12-05 |
| Inactivation Date | 2020-01-31 |
| Ingredient | Strength |
|---|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 15 mg/5mL |
| SPL SET ID: | 8a6eb670-8bed-4941-b4fd-70b3f1e48401 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |