G-Tuss-NL is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Mclaren Medical. The primary component is Dextromethorphan Hydrobromide; Guaifenesin; Pseudoephedrine Hydrochloride.
| Product ID | 43913-404_2dfe9515-b626-41d6-a129-5054814af76f |
| NDC | 43913-404 |
| Product Type | Human Otc Drug |
| Proprietary Name | G-Tuss-NL |
| Generic Name | Dextromethorphan Hydrobromide, Guaifenesin, And Pseudoephedrine Hydrochloride |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 2014-02-11 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | McLaren Medical |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Ingredient Strength | 10 mg/5mL; mg/5mL; mg/5mL |
| NDC Exclude Flag | E |
| Listing Certified Through | 2017-12-31 |
| Marketing Start Date | 2014-02-11 |
| NDC Exclude Flag | N |
| Sample Package? | N |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2014-02-11 |
| Inactivation Date | 2019-11-27 |
| Ingredient | Strength |
|---|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 10 mg/5mL |
| SPL SET ID: | 9de95fbd-e53c-41bc-9a88-819cbfb6f190 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 43913-404 | G-Tuss-NL | Dextromethorphan Hydrobromide, Guaifenesin, and Pseudoephedrine Hydrochloride |
| 43913-406 | G-Tuss-NL Ped | Dextromethorphan Hydrobromide, Guaifenesin, and Pseudoephedrine Hydrochloride |
| 43913-407 | G-Xpect PSE | Dextromethorphan Hydrobromide, Guaifenesin, and Pseudoephedrine Hydrochloride |