| NDC Code: |
58809-907 |
| Proprietary Name: |
VANACOF |
| Suffix: |
DX |
| Non-Proprietary Name: |
Chlophedianol Hydrochloride, Guaifenesin, and Pseudoephedrine Hydrochloride |
| Dosage Form: |
LIQUID |
| Method: |
ORAL |
| Original Marketing Date: |
23-04-2008 |
| Category Name: |
OTC MONOGRAPH FINAL |
| Application Number: |
part341 |
| Labeler: |
GM PHARMACEUTICALS |
| Substance Name: |
CHLOPHEDIANOL HYDROCHLORIDE; GUAIFENESIN; PSEUDOEPHEDRINE HYDROCHLORIDE |
| Active Numerator Strength: |
12.5; 100; 30 |
| Active Ingredient Unit: |
mg/5mL; mg/5mL; mg/5mL |
| Pharm Classes: |
|
| DEA Schedule: |
|
