Product NDC: | 0485-0080 |
Proprietary Name: | RYMED |
Non Proprietary Name: | DEXCHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 2; 10 mg/1; mg/1 & nbsp; DEXCHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0485-0080 |
Labeler Name: | EDWARDS PHARMACEUTICALS, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20111115 |
Package NDC: | 0485-0080-01 |
Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0485-0080-01) |
NDC Code | 0485-0080-01 |
Proprietary Name | RYMED |
Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0485-0080-01) |
Product NDC | 0485-0080 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DEXCHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20111115 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | EDWARDS PHARMACEUTICALS, INC. |
Substance Name | DEXCHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 2; 10 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |