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) |
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 NDC: | 52083-237-04 |
Package Description: | 120 mL in 1 BOTTLE (52083-237-04) |
NDC Code | 52083-237-04 |
Proprietary Name | Tussi Pres B |
Package Description | 120 mL in 1 BOTTLE (52083-237-04) |
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 |