Product NDC: | 0067-2083 |
Proprietary Name: | COMTREX |
Non Proprietary Name: | Acetaminophen, Chlorpheniramine Maleate, Phenylephrin HCl |
Active Ingredient(s): | & nbsp; Acetaminophen, Chlorpheniramine Maleate, Phenylephrin HCl |
Administration Route(s): | |
Dosage Form(s): | KIT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0067-2083 |
Labeler Name: | Novartis Consumer Health, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100701 |
Package NDC: | 0067-2083-24 |
Package Description: | 3 BLISTER PACK in 1 CARTON (0067-2083-24) > 1 KIT in 1 BLISTER PACK |
NDC Code | 0067-2083-24 |
Proprietary Name | COMTREX |
Package Description | 3 BLISTER PACK in 1 CARTON (0067-2083-24) > 1 KIT in 1 BLISTER PACK |
Product NDC | 0067-2083 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen, Chlorpheniramine Maleate, Phenylephrin HCl |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100701 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Novartis Consumer Health, Inc. |
Substance Name | |
Strength Number | |
Strength Unit | |
Pharmaceutical Classes |