Product NDC: | 66007-204 |
Proprietary Name: | Expectorant plus Cough Relief |
Non Proprietary Name: | Guaifenesin and Dextromethorphan |
Active Ingredient(s): | 5; 100 mg/1; mg/1 & nbsp; Guaifenesin and Dextromethorphan |
Administration Route(s): | ORAL |
Dosage Form(s): | GRANULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66007-204 |
Labeler Name: | Capricorn Pharma Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100806 |
Package NDC: | 66007-204-01 |
Package Description: | 12 GRANULE in 1 CARTON (66007-204-01) |
NDC Code | 66007-204-01 |
Proprietary Name | Expectorant plus Cough Relief |
Package Description | 12 GRANULE in 1 CARTON (66007-204-01) |
Product NDC | 66007-204 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Guaifenesin and Dextromethorphan |
Dosage Form Name | GRANULE |
Route Name | ORAL |
Start Marketing Date | 20100806 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Capricorn Pharma Inc. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 5; 100 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |