Product NDC: | 49789-030 |
Proprietary Name: | CAREPANTO |
Non Proprietary Name: | DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE |
Active Ingredient(s): | 3; 15 mg/630mg; mg/630mg & nbsp; DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49789-030 |
Labeler Name: | SAMSUNG PHARM IND. CO., LTD. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120301 |
Package NDC: | 49789-030-01 |
Package Description: | 630 mg in 1 BLISTER PACK (49789-030-01) |
NDC Code | 49789-030-01 |
Proprietary Name | CAREPANTO |
Package Description | 630 mg in 1 BLISTER PACK (49789-030-01) |
Product NDC | 49789-030 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DEXTROMETHORPHAN HYDROBROMIDE, CHLORPHENIRAMINE MALEATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120301 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | SAMSUNG PHARM IND. CO., LTD. |
Substance Name | CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE |
Strength Number | 3; 15 |
Strength Unit | mg/630mg; mg/630mg |
Pharmaceutical Classes |