Product NDC: | 17714-016 |
Proprietary Name: | Anti Allergy |
Non Proprietary Name: | Chlorpheniramine Maleate |
Active Ingredient(s): | 4 mg/1 & nbsp; Chlorpheniramine Maleate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17714-016 |
Labeler Name: | Advance Pharmaceutical Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20020109 |
Package NDC: | 17714-016-01 |
Package Description: | 100 TABLET in 1 BOTTLE (17714-016-01) |
NDC Code | 17714-016-01 |
Proprietary Name | Anti Allergy |
Package Description | 100 TABLET in 1 BOTTLE (17714-016-01) |
Product NDC | 17714-016 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Chlorpheniramine Maleate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20020109 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Advance Pharmaceutical Inc. |
Substance Name | CHLORPHENIRAMINE MALEATE |
Strength Number | 4 |
Strength Unit | mg/1 |
Pharmaceutical Classes |