Diphenhydramine Hydrochloride 17714-0135
Product NDC
17714-0135- Manufacturer
- Advance Pharmaceutical Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Otc Drug
- Marketing Start
- September 26, 2006
- Listing Expires
- December 31, 2026
- Application
- part341
Active Ingredients
| Ingredient | Strength |
|---|---|
| Diphenhydramine Hydrochloride | 25 mg/1 |
Drug Class
Histamine H1 Receptor Antagonists [MoA]Histamine-1 Receptor Antagonist [EPC]
Packaging Options(1)
100 TABLET in 1 BOTTLE (17714-135-01)