Product NDC: | 0485-0204 |
Proprietary Name: | Rynex |
Non Proprietary Name: | Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
Active Ingredient(s): | 1; 5; 2.5 mg/5mL; mg/5mL; mg/5mL & nbsp; Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0485-0204 |
Labeler Name: | Edwards Pharmaceuticals, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110314 |
Package NDC: | 0485-0204-10 |
Package Description: | 10 mL in 1 BOTTLE (0485-0204-10) |
NDC Code | 0485-0204-10 |
Proprietary Name | Rynex |
Package Description | 10 mL in 1 BOTTLE (0485-0204-10) |
Product NDC | 0485-0204 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Brompheniramine Maleate, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20110314 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Edwards Pharmaceuticals, Inc |
Substance Name | BROMPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 1; 5; 2.5 |
Strength Unit | mg/5mL; mg/5mL; mg/5mL |
Pharmaceutical Classes |