TUSICOF is a Oral Syrup in the Human Otc Drug category. It is labeled and distributed by Kramer Novis. The primary component is Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride.
| Product ID | 52083-239_01045808-544c-4b23-88dc-041e37c3e19f |
| NDC | 52083-239 |
| Product Type | Human Otc Drug |
| Proprietary Name | TUSICOF |
| Generic Name | Dextromethorphan, Guaifenesin, And Phenylephrine |
| Dosage Form | Syrup |
| Route of Administration | ORAL |
| Marketing Start Date | 2010-08-17 |
| Marketing Category | OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Labeler Name | Kramer Novis |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient Strength | 20 mg/5mL; mg/5mL; mg/5mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2019-12-31 |
| Marketing Start Date | 2010-08-17 |
| 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 | 2012-10-08 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Billing Unit | ML |
| Marketing Start Date | 2010-08-17 |
| Marketing Category | OTC monograph final |
| Application Number | part341 |
| Product Type | HUMAN OTC DRUG |
| Marketing Start Date | 2010-08-17 |
| Ingredient | Strength |
|---|---|
| DEXTROMETHORPHAN HYDROBROMIDE | 20 mg/5mL |
| SPL SET ID: | e966b75c-4bb4-4216-8247-baada8f5d759 |
| Manufacturer | |
| UNII | |
| RxNorm Concept Unique ID - RxCUI | |
| UPC Code |
| NDC | Brand Name | Generic Name |
|---|---|---|
| 52083-239 | TUSICOF | dextromethorphan, guaifenesin, and phenylephrine |
| 52083-289 | Tusicof | Guaifenesin, phenylephrine HCL, Dextromethorphan |
| 52083-639 | G-TUSICOF | dextromethorphan, guaifenesin, and phenylephrine |