Product NDC: | 49580-0434 |
Proprietary Name: | Tussin Sugar Free Cough |
Non Proprietary Name: | Robitussin Sugar Free Cough |
Active Ingredient(s): | 10; 100 mg/5mL; mg/5mL & nbsp; Robitussin Sugar Free Cough |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49580-0434 |
Labeler Name: | Aaron Industries, Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080924 |
Package NDC: | 49580-0434-4 |
Package Description: | 118 mL in 1 BOTTLE, PLASTIC (49580-0434-4) |
NDC Code | 49580-0434-4 |
Proprietary Name | Tussin Sugar Free Cough |
Package Description | 118 mL in 1 BOTTLE, PLASTIC (49580-0434-4) |
Product NDC | 49580-0434 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Robitussin Sugar Free Cough |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20080924 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Aaron Industries, Inc. |
Substance Name | DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN |
Strength Number | 10; 100 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes |