Product NDC: | 59779-919 |
Proprietary Name: | tussin dm |
Non Proprietary Name: | Dextromethorphan HBr, Guaifenesin |
Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Dextromethorphan HBr, Guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-919 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 19941207 |
Package NDC: | 59779-919-34 |
Package Description: | 1 BOTTLE in 1 CARTON (59779-919-34) > 237 mL in 1 BOTTLE |
NDC Code | 59779-919-34 |
Proprietary Name | tussin dm |
Package Description | 1 BOTTLE in 1 CARTON (59779-919-34) > 237 mL in 1 BOTTLE |
Product NDC | 59779-919 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Dextromethorphan HBr, Guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19941207 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS Pharmacy |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 10; 100 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |