Excedrin - Acetaminophen, Diphenhydramine Citrate
Navigation: NDC > Supplier starting with: N > NOVARTIS CONSUMER HEALTH, INC.| Field | Value |
|---|---|
| NDC Code: | 0067-2055 |
| Proprietary Name: | Excedrin |
| Suffix: | PM |
| Non-Proprietary Name: | Acetaminophen, Diphenhydramine Citrate |
| Dosage Form: | TABLET, FILM COATED |
| Method: | ORAL |
| Original Marketing Date: | 01-07-2009 |
| Category Name: | OTC MONOGRAPH FINAL |
| Application Number: | part343 |
| Labeler: | NOVARTIS CONSUMER HEALTH, INC. |
| Substance Name: | ACETAMINOPHEN; DIPHENHYDRAMINE CITRATE |
| Active Numerator Strength: | 500; 38 |
| Active Ingredient Unit: | mg/1; mg/1 |
| Pharm Classes: | |
| DEA Schedule: |