| Product NDC: | 49580-3412 |
| Proprietary Name: | Tussin Cough Long Acting |
| Non Proprietary Name: | Robitussin Cough Long Acting |
| Active Ingredient(s): | 10 mg/5mL & nbsp; Robitussin Cough Long Acting |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49580-3412 |
| Labeler Name: | Aaron Industries Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part341 |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20100113 |
| Package NDC: | 49580-3412-4 |
| Package Description: | 118 mL in 1 BOTTLE, PLASTIC (49580-3412-4) |
| NDC Code | 49580-3412-4 |
| Proprietary Name | Tussin Cough Long Acting |
| Package Description | 118 mL in 1 BOTTLE, PLASTIC (49580-3412-4) |
| Product NDC | 49580-3412 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Robitussin Cough Long Acting |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100113 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Aaron Industries Inc |
| Substance Name | DEXTROMETHORPHAN HYDROBROMIDE |
| Strength Number | 10 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |