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Tussi Pres
Tussi Pres - 52083-233-04 - (guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide)
Drug Information of Tussi Pres
| Product NDC: | 52083-233 |
| Proprietary Name: | Tussi Pres |
| Non Proprietary Name: | guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide |
| Active Ingredient(s): | 10; 200; 5 mg/5mL; mg/5mL; mg/5mL & nbsp; guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tussi Pres
| Product NDC: | 52083-233 |
| Labeler Name: | Kramer Novis |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110328 |
Package Information of Tussi Pres
| Package NDC: | 52083-233-04 |
| Package Description: | 120 mL in 1 BOTTLE (52083-233-04) |
NDC Information of Tussi Pres
| NDC Code | 52083-233-04 |
| Proprietary Name | Tussi Pres |
| Package Description | 120 mL in 1 BOTTLE (52083-233-04) |
| Product NDC | 52083-233 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | guaifenesin, phenylephrine hydrochloride, dextromethorphan hydrobromide |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20110328 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kramer Novis |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 10; 200; 5 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
