| NDC Code: |
49580-0126 |
| Proprietary Name: |
Tussin CF |
| Suffix: |
Dextromethorphan HBr, Guaifenesin, Phenylephrine HCL |
| Non-Proprietary Name: |
Robitussin CF |
| Dosage Form: |
LIQUID |
| Method: |
ORAL |
| Original Marketing Date: |
10-01-2005 |
| Category Name: |
OTC MONOGRAPH FINAL |
| Application Number: |
part341 |
| Labeler: |
AARON INDUSTRIES INC |
| Substance Name: |
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Numerator Strength: |
10; 100; 5 |
| Active Ingredient Unit: |
mg/5mL; mg/5mL; mg/5mL |
| Pharm Classes: |
|
| DEA Schedule: |
|
