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COMTREX
COMTREX - 0067-2077-24 - (Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl)
Drug Information of COMTREX
| Product NDC: | 0067-2077 |
| Proprietary Name: | COMTREX |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| Active Ingredient(s): | 325; 10; 15 mg/1; mg/1; mg/1 & nbsp; Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of COMTREX
| Product NDC: | 0067-2077 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20061208 |
Package Information of COMTREX
| Package NDC: | 0067-2077-24 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (0067-2077-24) > 12 TABLET, COATED in 1 BLISTER PACK |
NDC Information of COMTREX
| NDC Code | 0067-2077-24 |
| Proprietary Name | COMTREX |
| Package Description | 2 BLISTER PACK in 1 CARTON (0067-2077-24) > 12 TABLET, COATED in 1 BLISTER PACK |
| Product NDC | 0067-2077 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl |
| Dosage Form Name | TABLET, COATED |
| Route Name | ORAL |
| Start Marketing Date | 20061208 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 325; 10; 15 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes |
