| NDC Code: |
52083-249 |
| Proprietary Name: |
Guaifenesin Phenylephrine Dextromethorphan |
| Suffix: |
|
| Non-Proprietary Name: |
Guaifenesin, phenylephrine HCL, Dextromethorphan |
| Dosage Form: |
TABLET, COATED |
| Method: |
ORAL |
| Original Marketing Date: |
18-07-2012 |
| Category Name: |
OTC MONOGRAPH FINAL |
| Application Number: |
part341 |
| Labeler: |
KRAMER NOVIS. |
| Substance Name: |
DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE |
| Active Numerator Strength: |
20; 400; 10 |
| Active Ingredient Unit: |
mg/1; mg/1; mg/1 |
| Pharm Classes: |
|
| DEA Schedule: |
|
