Product NDC: | 0485-0085 |
Proprietary Name: | ED-CHLORTAN |
Non Proprietary Name: | CHLORPHENIRAMINE MALEATE |
Active Ingredient(s): | 4 mg/1 & nbsp; CHLORPHENIRAMINE MALEATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0485-0085 |
Labeler Name: | EDWARDS PHARMACEUTICALS, INC. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20110607 |
Package NDC: | 0485-0085-01 |
Package Description: | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0485-0085-01) |
NDC Code | 0485-0085-01 |
Proprietary Name | ED-CHLORTAN |
Package Description | 100 TABLET, COATED in 1 BOTTLE, PLASTIC (0485-0085-01) |
Product NDC | 0485-0085 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CHLORPHENIRAMINE MALEATE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20110607 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | EDWARDS PHARMACEUTICALS, INC. |
Substance Name | CHLORPHENIRAMINE MALEATE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes |