Product NDC: | 0485-0096 |
Proprietary Name: | ED CHLORPED D |
Non Proprietary Name: | CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 2; 5 mg/mL; mg/mL & nbsp; CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0485-0096 |
Labeler Name: | EDWARDS PHARMACEUTICALS, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110601 |
Package NDC: | 0485-0096-02 |
Package Description: | 60 mL in 1 BOTTLE, DROPPER (0485-0096-02) |
NDC Code | 0485-0096-02 |
Proprietary Name | ED CHLORPED D |
Package Description | 60 mL in 1 BOTTLE, DROPPER (0485-0096-02) |
Product NDC | 0485-0096 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CHLORPHENIRAMINE MALEATE and PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20110601 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | EDWARDS PHARMACEUTICALS, INC. |
Substance Name | CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 2; 5 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |