Product NDC: | 61715-013 |
Proprietary Name: | Preferred Plus Chest Congestion Relief DMTDM |
Non Proprietary Name: | Dextromethorphan Hydrobromide / Guaifenesin |
Active Ingredient(s): | 20; 400 mg/1; mg/1 & nbsp; Dextromethorphan Hydrobromide / Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61715-013 |
Labeler Name: | Kinray |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120801 |
Package NDC: | 61715-013-50 |
Package Description: | 50 TABLET in 1 BOTTLE, PLASTIC (61715-013-50) |
NDC Code | 61715-013-50 |
Proprietary Name | Preferred Plus Chest Congestion Relief DMTDM |
Package Description | 50 TABLET in 1 BOTTLE, PLASTIC (61715-013-50) |
Product NDC | 61715-013 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan Hydrobromide / Guaifenesin |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20120801 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Kinray |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 20; 400 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |