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Tussi Pres B
Tussi Pres B - 52083-237-01 - (dextromethorphan hydrobromide, brompheniramine maleate, phenylephrine hydrochloride)
Drug Information of Tussi Pres B
| Product NDC: | 52083-237 |
| Proprietary Name: | Tussi Pres B |
| Non Proprietary Name: | dextromethorphan hydrobromide, brompheniramine maleate, phenylephrine hydrochloride |
| Active Ingredient(s): | 4; 20; 10 mg/5mL; mg/5mL; mg/5mL & nbsp; dextromethorphan hydrobromide, brompheniramine maleate, phenylephrine hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tussi Pres B
| Product NDC: | 52083-237 |
| Labeler Name: | KRAMER NOVIS |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110329 |
Package Information of Tussi Pres B
| Package NDC: | 52083-237-01 |
| Package Description: | 30 mL in 1 BOTTLE (52083-237-01) |
NDC Information of Tussi Pres B
| NDC Code | 52083-237-01 |
| Proprietary Name | Tussi Pres B |
| Package Description | 30 mL in 1 BOTTLE (52083-237-01) |
| Product NDC | 52083-237 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | dextromethorphan hydrobromide, brompheniramine maleate, phenylephrine hydrochloride |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20110329 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | KRAMER NOVIS |
| Substance Name | BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 4; 20; 10 |
| Strength Unit | mg/5mL; mg/5mL; mg/5mL |
| Pharmaceutical Classes |
