| NDC Code: |
49348-737 |
| Proprietary Name: |
SUNMARK TUSSIN CF |
| Suffix: |
|
| Non-Proprietary Name: |
Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride |
| Dosage Form: |
LIQUID |
| Method: |
ORAL |
| Original Marketing Date: |
02-05-2006 |
| Category Name: |
OTC MONOGRAPH FINAL |
| Application Number: |
part341 |
| Labeler: |
MCKESSON |
| 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: |
|
