| NDC Code: |
70253-142 |
| Proprietary Name: |
Day Time |
| Suffix: |
with PE |
| Non-Proprietary Name: |
Acetaminophen, Dextromethorphan Hydrobromide, Phenylephrine Hydrochloride |
| Dosage Form: |
LIQUID |
| Method: |
ORAL |
| Original Marketing Date: |
02-01-2007 |
| Category Name: |
OTC MONOGRAPH FINAL |
| Application Number: |
part341 |
| Labeler: |
NASH FINCH COMPANY |
| Substance Name: |
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE |
| Active Numerator Strength: |
325; 10; 5 |
| Active Ingredient Unit: |
mg/15mL; mg/15mL; mg/15mL |
| Pharm Classes: |
|
| DEA Schedule: |
|
