Product NDC: | 0031-8712 |
Proprietary Name: | ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM |
Non Proprietary Name: | dextromethorphan HBr, guaifenesin |
Active Ingredient(s): | 2; 20 mg/mL; mg/mL & nbsp; dextromethorphan HBr, guaifenesin |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0031-8712 |
Labeler Name: | Richmond Division of Wyeth |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20070731 |
Package NDC: | 0031-8712-10 |
Package Description: | 10 POUCH in 1 BOX (0031-8712-10) > 10 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0031-8712-10 |
Proprietary Name | ROBITUSSIN TO GO COUGH AND CHEST CONGESTION DM |
Package Description | 10 POUCH in 1 BOX (0031-8712-10) > 10 VIAL, SINGLE-DOSE in 1 POUCH > 10 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0031-8712 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | dextromethorphan HBr, guaifenesin |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20070731 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Richmond Division of Wyeth |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 2; 20 |
Strength Unit | mg/mL; mg/mL |
Pharmaceutical Classes |